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Publications

2022

367. Towards Substrate-Reagent Interaction of Lochmann-Schlosser Bases in THF: Bridging THF Hides Potential Reaction Site of a Chiral Superbase:
L. Brieger, T. Schrimpf, R. Scheel, C. Unkelbach, C. Strohmann,
Chem. Eur. J. 2022, accepted.

366. Tris(µ2-carbonyl)octacarbonyl(triphenylphosphite)tetracobalt:
I. Jourdain, M. Knorr, C. Strohmann, R. Scheel,
Molbank 2022, 2022, M1443.

365. Chemoselective and diastereodivergent synthesis of new spirooxindolo-pyrrolizidines and pyrrolidines stemming from unsymmetrical 1,3-bis(arylidene)tetral-2-ones: A combined experimental and theoretical study:
H. Gazzeh, F. Rouatbi, S. Chniti, M. Askri, M. Knorr, C. Strohmann, C. Golz, A.M. Lamsabhi,
New J. Chem. 2022, 46, accepted.

364. Identification of a Novel Pseudo-Natural Product Type IV IDO1 Inhibitor Chemotype:
C. Davies, L. Dötsch, M.G. Ciulla, E. Hennes, K. Yoshida, R. Gasper, R. Scheel, S. Sievers, C. Strohmann, K. Kumar, S. Ziegler, H. Waldmann,
Angew. Chem. Int. Ed. 2022, accepted;
Angew. Chem. 2022, accepted.

363. Chain Length Effect on the Structural and Emission Properties of the CuI/Bis((4-methoxyphenyl)thio)alkane Coordination Polymers:
A. Schlachter, R. Scheel, D. Fortin, C. Strohmann, M. Knorr, P.D. Harvey,
Inorg. Chem. 2022, 61 , 11306–11318.

362. Design of Novel Enantiopure Dispirooxindolopyrrolidine-Piperidones as Promising Candidates toward COVID-19: Asymmetric Synthesis, Crystal Structure and In Silico Studies:
A. Toumi, S. Boudriga, Y.M. Mandour, A.A. Mekki, M. Knorr, C. Strohmann, J.-L. Kirchhoff, M. Sobeh,
Molecules 2022, 27, 3945.

361. Bis(μ-iodo)-tetrakis(O-methyl N-phenylthiocarbamate)-tetraiodo-dibismuth:
W. Arar, A. Khatyr, M. Knorr, C. Strohmann, A. Schmidt,
Molbank 2022, 2022, M1381.

360. 2,2’-Ethylenebis(1,3-dithiane) as polydentate μ2-, μ4- and μ5-assembling ligand for the construction of sulphur-rich Cu(I), Hg(II) and heterometallic Cu(I)/Hg(II) coordination polymers featuring uncommon network architectures:
L. Viau, M. Knorr, L. Knauer, L. Brieger, C. Strohmann,
Dalton Trans. 2022, 51, 7581-7606.

359. The Pseudo-Natural Product Rhonin Targets RHOGDI:
H. Waldmann, M. Akbarzadeh, J. Flegel, S. Patil, E. Shang, R. Narayan, M. Buchholzer, N.S.K. Jasemi, M. Grigalunas, A. Krzyzanowski, D. Abegg, A. Shuster, M. Potowski, H. Karatas, G. Karageorgis, N. Mosaddeghzadeh, M.-L. Zischinsky, C. Merten, C. Golz, L. Brieger, C. Strohmann, A.P. Antonchick, P. Janning, A. Adibekian, R.S. Goody, M.R. Ahmadian, S. Ziegler,
Angew. Chem. Int. Ed. 2022, 61, e202115193;
Angew. Chem. 2022, 134, e202115193.

358. Antimicrobial Activity and DFT Studies of a Novel Set of Spiropyrrolidines Tethered with Thiochroman-4-one/Chroman-4-one Scaffolds:
N. Chouchène, A. Toumi, S. Boudriga, H. Edziri, M. Sobeh, Mohamed A.O. Abdelfattah, M. Askri, M. Knorr, C. Strohmann, L. Brieger, A. Soldera,
Molecules 2022, 27, 582.

357. New spiropyrrolothiazole derivatives bearing an oxazolone moiety as potential antidiabetic agent: Design, synthesis, crystal structure, Hirshfeld surface analysis, ADME and molecular docking studies:
M. Ben Mahmmoud, S. Boudriga, K. Hamden, M. Askri, M. Knorr, C. Strohmann, L. Brieger, A. Krupp, El H. Anouar, M. Snoussi, K Aouadi, A. Kadri,
J. Mol. Struct. 2022, 1254, 132398.

356. Crystal structure and Hirshfeld surface analysis of 1-[(benzyldimethylsilyl)methyl]-1-ethylpiperidin-1-ium ethanesulfonate:
J.-L. Kirchhoff, S.G. Koller, K. Louven, C. Strohmann,
Acta Cryst. 2022, E78, 135-139.

355. Crystal structure and Hirshfeld surface analysis of (S)-N-methyl-1-phenylethan-1-aminium chloride:
J.-L. Kirchhoff, L. Brieger, C. Strohmann,
Acta Cryst. 2022, E78, 130-134.

354. Crystal structure of N,N,N′,N′-tetramethylethanediamine:
T. Schrimpf, F. Otte, C. Strohmann,
Acta Cryst. 2022, E78, 36-39.

353. Crystal structures and Hirshfeld surface analyses of bis­(4,5-dihydrofuran-2-yl)dimethylsilane and (4,5-dihydrofuran-2-yl)(methyl)diphenylsilane:
A. Schmidt, A. Krupp, E.R. Barth, C. Strohmann,
Acta Cryst. 2022, E78, 23-28.

352. Design of hydroxyl- and thioether-functionalized iron-platinum dimetallacyclopentenone complexes. Crystal and electronic structures, Hirshfeld and docking analyses and anticancer activity evaluated by In silico simulation:
A. S. Mohamed, I. Jourdain, M. Knorr, A. Elmi, S. Chtita, R. Scheel, C. Strohmann, M. A. Hussien,
J. Mol. Struct. 2022, 1251, 131979.

2021

351. Stereoselective Synthesis of Cyclobutanes by Contraction of Pyrrolidines:
C. Hui, L. Brieger, C. Strohmann, A.P. Antonchick,
J. Am. Chem. Soc. 2021143, 18864-18870.

350. THF-solvated Heavy Alkali Metal Benzyl Compounds (Na, Rb, Cs): Defined Deprotonation Reagents for Alkali Metal Mediation Chemistry:
L. Brieger, C. Unkelbach, C. Strohmann,
Chem. Eur. J. 2021, 27, 17780-17784.

349. Diversity-Oriented Synthesis of Spiropyrrolo[1,2-a]isoquinoline Derivatives via Diastereoselective and Regiodivergent Three-Component 1,3-Dipolar Cycloaddition Reactions: In Vitro and in Vivo Evaluation of the Antidiabetic Activity of Rhodanine Analogues:
A. Toumi, S. Boudriga, K. Hamden, I. Daoud, M. Askri, A. Soldera, J.-F. Lohier, C. Strohmann, L. Brieger, M. Knorr,
J. Org. Chem. 2021, 86, 13420–13445.

348. Combination of Pseudo-Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo-Sesquiterpenoid Alkaloids:
J. Liu, J. Flegel, F. Otte, A. Pahl, S. Sievers, C. Strohmann, H. Waldmann,
Angew. Chem. Int. Ed. 2021, 60, 21384-21395;
Angew. Chem. 2021, 133, 21554-21565.

347. A Fused Poly(truncated rhombic dodecahedron)-containing 3D-Coordination Polymer: A Multifunctional Material With Exceptional Properties:
A. Schlachter, K. Tanner, R. Scheel, P.-L. Karsenti, C. Strohmann, M. Knorr, P.D. Harvey,
Inorg. Chem. 2021, 60 , 13528–13538.

346. Synthesis of Indofulvin Pseudo-Natural Products Yields a New Autophagy Inhibitor Chemotype:
A. Burhop, S. Bag, M. Grigalunas, S. Woitalla, P. Bodenbinder, L. Brieger, C. Strohmann, A. Pahl, S. Sievers, H. Waldmann,
Adv. Sci. 2021, 8, 2102042.

345. Cascade aza-Wittig/6π-Electrocyclization in the Synthesis of 1,6-Dihydropyridines:
V. Polychronidou, A. Krupp, C. Strohmann, A.P. Antonchick,
Org. Lett. 2021, 23, 6024-6029.

344. Dynamic Catalytic Highly Enantioselective 1,3-Dipolar Cycloadditions:
O. Yildirim, M. Grigalunas, L. Brieger, C. Strohmann, A.P. Antonchick, H. Waldmann,
Angew. Chem. Int. Ed. 2021, 60, 20012-20020;
Angew. Chem. 2021, 133,
20165-20173.

343. Primary Amine Functionalization of Alkoxysilanes: Synthesis, Selectivity and Mechanistic Insights:
M. Achternbosch, L. Zibula, J.-L. Kirchhoff, J. O. Bauer, C. Strohmann,
Inorg. Chem. 2021, 60, 11562–11568.

342. Enantioselective synthesis of pyrro[3,4-c]quinoline pseudo-natural products:
J. Liu, F. Otte, C. Strohmann, H. Waldmann,
Tetrahedron Letters 2021, 76, 153228.

341. Crystal structures of 9-[bis­(benzyl­sulfanyl)methyl]anthracene and of cyclo-dodeca­kis­(μ2-phenyl­methanethiolato-κ2S:S)hexapalladium(6 Pd—Pd)–anthracene-9,10-dione (1/1):
A. Raghuvanshi, A. Krupp, L. Viau, M. Knorr, C. Strohmann,
Acta Cryst. 2021, E77, 718-725.

340. Cytotoxic Compounds from the Stem Bark of Two subsp. of Bersama abyssinica:
D.K. Nyamboki, K.G. Bedane, K. Hassan, L. Brieger, C. Strohmann, M. Spiteller, J.C. Matasyoh,
J. Nat. Prod. 2021, 84, 1453–1458.

339. Synthesis, Crystal Structures and Hirshfeld Analyses of Phosphonothioamidates (EtO)2P(=O)C(=S)N(H)R (R = Cy, Bz) and their Coordination on CuI and HgX2 (X = Br, I):
W. Arar, A. Khatyr, M. Knorr, L. Brieger, A. Krupp, C. Strohmann, M. Lotfi Efrit, A. Ben Akacha,
Phosphorus, Sulfur, and Silicon and the Related Elements 2021, 196, 845–858.

338. Electrochemical Dehydrogenative C(sp2)-H Amination:
M. Puthanveedu, V. Khamraev, L. Brieger, C. Strohmann, A.P. Antonchick,
Chem. Eur. J. 2021, 27, 8008-8012.

337. Influence Of Lithium Coordinating Additives On The Structure Of Phenyldimethylsilyllithium:
M. Achternbosch, L. Brieger, C. Strohmann,
Z. Anorg. Allg. Chem. 2021, 647, 979-983.

336. Natural Product Fragment Combination to Performance-Diverse Pseudo-Natural Products:
M. Grigalunas, A. Burhop, S. Zinken, A. Pahl, J.M. Gally, N. Wild, Y. Mantel, S. Sievers, D. Foley, R. Scheel, C. Strohmann, A. Antonchick, H. Waldmann,
Nature Commun. 2021, 12, 1883-1993.

335. Weak yet Decisive: Molecular Halogen Bond and Competing Weak Interactions of Iodobenzene and Quinuclidine:
F. Otte, J. Kleinheider, W. Hiller, R. Wang, U. Englert, C. Strohmann,
J. Am. Chem. Soc. 2021, 143, 4133–4137.

334. When Electrons Step in: Polarizing Effects Explored with Triisobutylaluminum:
A. Hermann, A. Münch, S.A. Orr, R. Herbst-Irmer, R.E. Mulvey, C. Strohmann, D. Stalke,
Inorg. Chem. 2021, 60, 2872–2877.

333. 2-Azabutadiene Complexes of Rhenium(I): S,N-Chelated Species With Photophysical Properties Heavily Governed by the Ligand Hidden Traits:
A. Schlachter, F. Juvenal, R. Kinghat Tangou, A. Khatyr, F. Guyon, P.-L. Karsenti, C. Strohmann, M.M. Kubicki, Y. Rousselin, P.D. Harvey, M. Knorr,
Dalton Trans. 2021, 50, 2945-2963.

332. Design, synthesis and biological evaluation of chemically and biologically diverse pyrroquinoline pseudo natural products: 
J. Liu, G.S. Cremosnik, F. Otte, A. Prahl, S. Sievers, C. Strohmann, H. Waldmann,
Angew. Chem. Int. Ed. 2021, 60, 4648-4656;
Angew. Chem. 2021, 133, 4698-4706.

 331. Synthesis, antidiabetic activity and molecular docking study of rhodamine-substitued spirooxindole pyrrolidine derivatives as novel α-amylase inhibitors:
A. Toumi, S. Boudriga, K. Hamden, M. Sobeh, M. Cheurfa, M. Askria, M. Knorr, C. Strohmann, L. Brieger,
Bioorg. Chem. 2021106, 104507.

330. Unusual Coordination Pattern of the Lithium Center in a Chiral α-Lithiated Silicon Compound:
J.O. Bauer, C. Strohmann, 
Organometallics 2021, 40, 11-15.

329. Aza-heterocyclic frameworks through intramolecular π-system trapping of spiro-N-acyliminiums generated from isoindolinone:
S. Chortani, M. Othman, A.M. Lawson, A. Romdhane, H. Ben Jannet, M. Knorr, L. Brieger, C. Strohmann, A. Daïch,
New J. Chem. 2021, 45, 2393-2403.

2020

328. Enantioselective Synthesis of Five-Membered-Ring Atropisomers with Chiral Rh(III) Complex:
S. Shaaban, H. Li, F. Otte, C. Strohmann, A. Antonchick, H. Waldmann,
Org. Lett. 2020, 22, 9199-9202.

327. Synthesis and Reactivity of Tris(arylphosphite)-ligated Cobalt Complexes [{ArO)3P}(OC)3Co-Co(CO)3{P(OAr)3}] and their Reactivity towards Phenylacetylene and Diphenylacetylene: 
I. Jourdain, M. Knorr, L. Brieger, C. Strohmann,
ACR 2020, 2.

326. The Structure-defining Incorporation of Chloride in Methyllithium Dimers:
L. Knauer, C. Strohmann,
Chem. Commun. 2020, 56, 13543-13546.

325. Anti-inflammatory steroidal sapogenins and a conjugated chalcone-stilbene from Dracaena usambarensis Engl.:
N.-N. Valderament-Alexe, L.K. Omosa, K.G. Bedane, S. Derese, L. Brieger, C. Strohmann, M. Spiteller,
Fitoterapia 2020, 146, 104717.

324. Crystal structures, Hirshfeld atom refinements and Hirshfeld surface analyses of tris­(4,5-dihydrofuran-2-yl)methylsilane and tris­(4,5-dihydrofuran-2-yl)phenylsilane:
A. Krupp, E.R. Barth, R. Seymen, C. Strohmann,
Acta Cryst. 2020, E76, 1514-1519.

323. Insight into the Bonding and Aggregation of Alkyllithiums by Experimental Charge Density Studies and Energy Decomposition Analyses:
A. Münch, L. Knauer, H. Ott, C.P. Sindlinger, R. Herbst-Irmer, C. Strohmann, D. Stalke,
J. Am. Chem. Soc. 2020, 142, 15897–15906.

322. Aminopotassiation by Mixed Potassium/Lithium Amides: A Synthetic Path to Difficult to Access Phenethylamine Derivates:
A. Hermann, U. Opper, A. Voß, L. Brieger, F. Otte, C. Unkelbach, D. O’Shea, C. Strohmann,
Angew. Chem. Int. Ed. 2020, 59, 22500-22504;
Angew. Chem. 2020, 132, 22688-22693.

321. Asymmetric Synthesis of 3,3′-Piperidinoyl Spirooxindoles and Discovery of Stereospecific Cycloadducts as Novel Hedgehog Pathway Modulators:
M. Rehan, J. Flegel, F. Heitkamp, J.L. Pergomet, F. Otte, C. Strohmann, K. Kumar,
Synthesis 2020, 52, 3140-3152.

320. Crystal structures of [(N,N-di­methyl­amino)­meth­yl]ferrocene and (Rp,Rp)-bis­{2-[(di­methyl­amino)­meth­yl]ferrocen­yl}di­methyl­silane:
A. Krupp, J. Wegge, F. Otte, J. Kleinheider, H. Wall, C. Strohmann,
Acta Cryst. 2020, E76, 1437-1441.

319. Cytotoxic bufadienolides from the leaves of a medicinal plant Melianthus comosus collected in South Africa:
K. G. Bedane, L. Brieger, C. Strohmann, E.-J. Seo, T. Efferth, M. Spiteller,
Bioorg. Chem. 2020, 102, 104102.

318. RhIII‐Catalyzed C−H Activation of Aryl Hydroxamates for the Synthesis of Isoindolinones:
S. Shaaban, C. Davies, C. Merten, J. Flegel, F. Otte, C. Strohmann, H. Waldmann,
Chem. Eur. J. 2020, 26, 10729-10734.

317. Cytotoxic Bufadienolides from the Leaves of Melianthus major:
K. Bedane, L. Brieger, C. Strohmann, E.-J. Seo, T. Efferth, M. Spiteller,
J. Nat. Prod. 2020, 83, 2122-2128.

316. Crystal structure of {μ2-1,2-bis­[(4-methylphenylsulfanyl]-3-oxoprop-1-ene-1,3-diyl-1:2κ2C3:C1}dicarbonyl-1κ2C-[μ2-methylenebis(di­phenylphosphane)-1:2κ2P:P′](tri-phenylphosphane-2κP)ironplatinum(Fe—Pt), [(OC)2Fe(μ-dppm){μ-C(=O)C(4-MeC6H4SCH2)=CCH2SC6H4Me-4}Pt(PPh3)]:
A. Said Mohamed, I. Jourdain, M. Knorr, L. Brieger, C. Strohmann,
Acta Cryst. 2020, E76, 1087-1091.

315. Synthesis and crystal structure of [Zn6Br4(C9H18NO)4(OH)4]·2C3H6O2:
R. Scheel, L. Brieger, K. Louven, C. Strohmann,
Acta Cryst. 2020, E76, 998-1002.

314. Crystal structures of [Li7(i-PrO)3(C4H10NO)3]2O and [Na(iPrOH)2(C8H18NO2)]2:
R. Scheel, K. Louven, C. Strohmann,
Acta Cryst. 2020, E76, 948-953.

313. Three-component Access to Functionalized Spiropyrrolidine Heterocyclic Scaffolds and Their Cholinesterase Inhibitory Activity:
S. Boudriga, S. Haddad, V. Murugaiyah, M. Askri, M. Knorr, C. Strohmann, C. Golz,
Molecules 2020, 25, 1963-1984.

312. Influences of Steric Factors on the Reactivity and Structure of Diorganoalkoxysilylamides:
L. Zibula, M. Achternbosch, J. Wattenberg, F. Otte, C. Strohmann,
Z. Anorg. Allg. Chem. 2020, 646, 978-984.

311. From Short-bite Ligand Assembled Ribbons to Nanosized Networks in Cu(I) Coordination Polymers Built Upon Bis(benzylthio)alkanes (BzS(CH2)nSBz; n = 1-9:
A. Schlachter, A. Lapprand, D. Fortin, C. Strohmann, P.D. Harvey, M. Knorr,
Inorg. Chem. 2020, 59, 3686-3708.

310. Crystal structure of 2-[bis(benzylsulfanyl)methyl]-6-methoxyphenol:
A. Raghuvanshi, L. Knauer, L. Viau, M. Knorr, C. Strohmann,
Acta Cryst. 2020, E76, 484-487.

309. Crystal structure of 2-methyl-1,2,3,4-tetrahydroisoquinoline trihydrate:
F. Langenohl, F. Otte, C. Strohmann,
Acta Cryst. 2020, E76, 298-302.

308. Heteroleptic Coordination Environments in Metal-Mediated DNA G-Quadruplexes:
P.M. Punt, L.M. Stratmann, S. Sevim, L. Knauer, C. Strohmann, G.H. Clever,
Front. Chem. 2020, 8, 26.

307. Higher Carbon Analogues of 1,4-Dihydropyridines as Potent TGFβ/Smad Inhibitors:
E. R. Barth, D. Längle, F. Wesseler, C. Golz, A. Krupp, D. Schade, C. Strohmann,
Eur. J. Inorg. Chem. 2020, 176-181.

306. Crystal structure of the coordination polymer catena-poly[[[(acetonitrile-κN) copper(I)]-μ3-1,3-dithiolane-κ3S:S:S′] hexafluoridophosphate]:
L. Knauer, M. Knorr, L. Viau, C. Strohmann,
Acta Cryst. 2020, E76, 38-41.

2019

305. Crystal structure of dicarbonyl[μ2-methylenebis(diphenylphosphane)-κ2P:P′][μ2-2-(2,4,5-trimethylphenyl)-3-oxoprop-1-ene-1,3-diyl](triphenylphosphane-κP)ironplatinum(Fe-Pt)dichloromethane-toluene (1/1/2), [(OC)2Fe(μ-dppm)(μ-C(=O)C(2,4,5-C6H2Me3)=CH) Pt(PPh3)]:
L. Brieger, I. Jourdain, M. Knorr, C. Strohmann,
Acta Cryst. 2019, E75, 1902-1906.

304. Inhibition of Osimertinib-Resistant Epidermal Growth Factor Receptor EGFR-T790M/C797S:
J. Lategahn, M. Keul, P. Klövekorn, H.L. Tumbrink, J. Niggenaber, M.P. Müller, L. Hodson, M. Flaßhoff, J. Hardick, T. Grabe, J. Engel, C. Schultz-Fademrecht, M. Baumann, J. Ketzer, T. Mühlenberg, W. Hiller, G. Günther, A. Unger, H. Müller, A. Heimsoeth, C. Golz, B. Blank-Landeshammer, L. Kollipara, R.P. Zahedi, C. Strohmann, J.G. Hengstler, W.A.L. van Otterlo, S. Bauer, D. Rauh,
Chem. Sci. 2019, 10, 10789-10801.

303. A Scaffold Diversity Synthesis of Biologically Intriguing Cyclic Sulfonamides:
S. Zimmermann, M. Akbarzadeh, F. Otte, C. Strohmann, M.G. Sankar, S. Ziegler, A. Pahl, S. Sievers, K. Kumar,
Chem. Eur. J. 2019, 25, 15498-15503.

302. Inhibition of Glucose Transporters and Glutaminase Synergistically Impairs Tumor Cell Growth:
E.S. Reckzeh, G. Karageorgis, M. Schwalfenberg, J. Ceballos, J. Nowacki, M.C.M. Stroet, A. Binici, L. Knauer, S. Brand, A. Choidas, C. Strohmann, S. Ziegler, H. Waldmann,
Cell Chem. Biol. 2019, 26, 1214-1228.e25.

301. Redetermination of the crystal structure of tetrammineplatinum(II) dichloride - A microporous hydrogen-bonded 3D network exhibiting a temperature-dependent order-disorder phase transition:
L. Brieger, S. Henke, A. Said Mohamed, I. Jourdain, M. Knorr, C. Strohmann,
Inorg. Chim. Acta 2019, 495, 119002.

300. The smaller, the better? How aggregate size affects the reactivity of (trimethylsilyl)methyllithium:
L. Knauer, J. Wattenberg, U. Kroesen, C. Strohmann,
Dalton Trans. 2019, 48, 11285-11291.

299. Kinetically controlled asymmetric synthesis of silicon-stereogenic methoxy silanes using a planar chiral ferrocene backbone:
E.R. Barth, A. Krupp, F. Langenohl, L.Brieger, C. Strohmann,
Chem. Commun. 2019, 55, 6882-6885.

298. 1,3-Dithianes as assembling ligands for the construction of Cu(I) coordination polymers. Investigation of the impact of the RC(H)S2C3H6 substituent and reaction conditions on the architecture of the 0D-3D networks:
A. Raghuvanshi, M. Knorr, L. Knauer, C. Strohmann, S. Boullanger, V. Moutarlier, L. Viau,
Inorg. Chem. 2019, 58, 5753-5775.

297. Heterodinuclear Diphosphane-bridged Iron-Platinum Diyne Complexes as Metalloligands for the Assembly of Polymetallic Systems (Fe, Pt, Co):
A. Said Mohamed, I. Jourdain, M. Knorr, S. Boullanger, L. Brieger, C. Strohmann,
J. Clust. Sci. 2019, 30, 1211-1225.

296. Highly diastereoselective construction of novel dispiropyrrolo[2,1-a]isoquinoline derivatives via multicomponent 1,3-dipolar cycloaddition of cyclic diketones-based tetrahydroisoquinolinium N-ylides:
S. Boudriga, S. Haddad, M. Askri, A. Soldera, M. Knorr, C. Strohmann, C. Golz,
RSC Advances 2019, 9, 11082-110912.

295. Access to 3-spiroindolizines containing an isoindole ring through intra-molecular arylation of spiro-N-acyliminium species: a new family of potent farnesyltransferase inhibitors:
A. Pesquet, H. Marzag, M. Knorr, C. Strohmann, A. Martin Lawson, A. Ghinet, J. Dubois, F. Amaury, A. Daïch, M. Othman,
Org. Biomol. Chem. 2019, 17, 2798-2808.

294. Unravelling the Synthesis and Chemistry of Stable, Acyclic, and Double‐Deficient 1,3‐Butadienes: An endo‐Selective Diels–Alder Route to Hedgehog Pathway Inhibitors:
X.Xin, S.Zimmermann, J. Flegel, F. Otte, L. Knauer, C. Strohmann, S. Ziegler, K.Kumar,
Chem. Eur. J. 2019, 25, 2717-2722.

Archiv

293. Cardenolides and dihydro-β-agarofuran sesquiterpenes from the seeds of Salacia staudtiana:
D.W. Kamtcha, M. Tene, K.G. Bedande, L. Knauer, L. Brieger, C. Strohmann, P. Tane, S. Kusari, M. Spiteller,
Fitoterapia 2018, 131, 174-181.

292. Gold(I)-Catalyzed and Nucleophile-Guided Ligand-Directed Divergent Synthesis:
Y.-C. Lee, L. Knauer, K. Louven, C. Golz, C. Strohmann, H. Waldmann, K. Kumar,
Eur. J. Org. Chem. 2018, 2018, 5688-5699.

291. Control of Structures and Emission Properties of (CuI)n 2-Methyldithiane Coordination Polymers:
A. Schlachter, L. Viau, D. Fortin, L. Knauer, C. Strohmann, M. Knorr, P.D. Harveya,
Inorg. Chem. 2018, 57, 13564-13576.

290. Mechanistic Studies on the Organocatalytic α‐Chlorination of Aldehydes: The Role and Nature of Off‐Cycle Intermediates:
S. Ponath, M. Menger, L. Grothues, M. Weber, D. Lentz, C. Strohmann, M. Christmann,
Angew. Chem. Int. Ed. 2018, 57, 11683-11687.

289. Scaffold Diversity Synthesis Delivers Complex, Structurally, and Functionally Distinct Tetracyclic Benzopyrones:
M.G. Sankar, S. Roy, T. Thi Ngoc Tran, K. Wittstein, J.O. Bauer, C. Strohmann, S. Ziegler, K. Kumar,
ChemistryOpen 2018, 7, 302-309.

288. 1,2-bis(3,5-dimethylphenyl)ethane:
L. Brieger, C. Unkelbach, C. Strohmann,
IUCrData 2018, 3, x180636.

287. Cardenolides from the stem bark of Salacia staudtiana:
D.W. Kamtcha, M. Tene, K.G. Bedande, L. Knauer, C. Strohmann, P. Tane, S. Kusari, M. Spiteller,
Fitoterapia 2018, 127, 402-409.

286. Catalytic Enantioselective Synthesis of a Pyrrolizidine-Alkaloid-Inspired Compound Collection with Antiplasmodial Activity:
Z.-J. Jia, H. Takayama, Y. Futamura, H. Aono, J.O. Bauer, C. Strohmann, A. Antonchick, H. Osada, H. Waldmann,
J. Org. Chem. 2018, 83, 7033-7041.

285. Crystal structure and quantum-chemical calculations of a trimethylaluminium-THF adduct:
L. Brieger, A. Hermann, C. Unkelbach, C. Strohmann,
Acta Cryst. 2018, E74, 267-270.

284. One-pot four component domino strategy for the synthesis of novel spirooxindole pyrrolidine/pyrrolizidine-linked 1,2,3-triazoles conjugates via stereo- and regioselective [3+2] cycloaddition reaction derivatives: in vitro antibacterial and antifungal studies:
R. Sakly, H. Edziri, M. Askri, M. Knorr, C. Strohmann, M. Masturi,
Comptes Rendus Chimie 2018, 21, 41-53.

283. Synthesis and molecular structure of a zwitterionic ZnI2 silanolate:
J.O. Bauer, C. Strohmann,
Inorg. Chim. Acta 2018, 469, 133-135.

282. Molecular Structures of Enantiomerically Pure (S)-2-(Triphenylsilyl)- and (S)-2-(Methyldiphenylsilyl)pyrrolidinium Salts:
J.O. Bauer, C. Strohmann,
Inorganics 2017, 5, 88-95.

281. A Tunable and Enantioselective Hetero-Diels–Alder Reaction Provides Access to Distinct Piperidinoyl Spirooxindoles:
S. Jayakumar, K. Louven, C. Strohmann, K. Kumar,
Angew. Chem. Int. Ed. 2017, 56, 15945-15949.

280. (2R,4S,5S)-5-Hydroxy-4-methyl-3-oxohept-6-en-2-yl benzoate:
V. von Kiedrowski, C. God, L. Knauer, C. Strohmann, H. Preut, M. Hiersemann,
IUCrData 2017, 2, x171539.

279. Assembly of Coordination Polymers Using Thioether-Functionalized Octasilsesquioxanes: Occurrence of (CuX)n Clusters (X=Br and I) within 3D-POSS Networks:
A. Raghuvanshi, C. Strohmann, J.-B. Tissot, S. Clément, A. Mehdi, S. Richeter, L. Viau, M. Knorr,
Chem. Eur. J. 2017, 23, 16479-16483.

278. Stereoselective Synthesis of Trisubstituted Epoxides Marks the Route to Chiral Building Blocks with Quaternary Centers:
M. Garcia-Castro, M. Annamalai, C. Golz, C. Strohmann, K. Kumar,
Eur. J. Org. Chem. 2017, 5660-5665.

277. Controlling the coordination sphere of alkyllithiums results in selective reactions with allylic amines:
U. Kroesen, C. Unkelbach, D. Schildbach, C. Strohmann,
Angew. Chem. Int. Ed. 2017, 56, 14164-14168.

276. Biology-Oriented Synthesis of Decahydro-4,8-epoxyazulene Scaffolds:
J. Zhi-Jun, C. Merten, L. Knauer, S. Murarka, C. Strohmann, H. Waldmann,
Synlett 2017, 28, 2918-2922.

275. Synthesis of New Spirooxindole-Fused Isoxazoline/Triazole and Isoxazoline/Isoxazole Derivatives Three-Component 1,3-Dipolar Cycloaddition:
R. Sakly, H. Edziri, M. Askri, M. Knorr, K. Louven, C. Strohmann, M. Masturi,
J. Heterocyclic Chem. 2017, 54, 3554-3564.

274. Highly Enantioselective Catalytic Vinylogous Propargylation of Coumarins Yields a Novel Autophagy Inhibitor Class:
H. Waldmann, H. Xu, L. Laraia, L. Schneider, K. Louven, C. Strohmann, A.P. Antonchick,
Angew. Chem. Int. Ed. 2017, 56, 11232-11236.

273. 1,3-Dithiolane and 1,3-Ferrocenyl-dithiolane as Assembling Ligands for the Construction of Cu(I) Clusters and Coordination Polymers:
A. Raghuvanshi, N.J. Hamad, M. Knorr, L. Viau, C. Strohmann, L. Knauer,
J. Inorg. Organomet. Polymers and Materials 2017, 27, 1501-1513.

272. Exploring Planar Chiral Amino Siloxides:
C. Golz, P. Steffen, C. Strohmann,
Angew. Chem. Int. Ed. 2017, 56, 8295-8298.

271. Selective Si-C(sp3) Bond Cleavage in (Aminomethyl)silanes by Carbanionic Nucleophiles and its Sterochemical Course:
S.G. Koller, J.O. Bauer, C. Strohmann,
Angew. Chem. Int. Ed. 2017, 56, 7991-7994.

270. Antibacterial secondary metabolites from an endophytic fungus, Fusarium solani JK10:
J. Oppong Kyekyeku, S. Kusari, R.K. Adosraku, A. Bullach, C. Golz, C. Strohmann, M. Spiteller,
Fitoterapia 2017, 119, 108-114.

269. The Reactivity of Benzyl Lithium Species is Regulated by Intermediate Structures:
U. Kroesen, L. Knauer, C. Strohmann,
Angew. Chem. Int. Ed. 2017, 56, 6232-6235.

268. Experimental and Theoretical Studies on the Mechanism of the C-S bond activation of PdII Thiolate/Thioether Complexes:
S. Kumar, F. Guyon, M. Knorr, S. Labat, K. Miqueu, C. Golz, C. Strohmann,
Organometallics 2017, 36, 1303-1321.

267. Epigenetic Modulation of Endophytic Eupenicillium sp. LG41 by a Histone Deacetylase Inhibitor for Production of Decalin-Containing Compounds:
G. Li, S. Kusari, C. Golz, H. Laatsch, C. Strohmann, M. Spiteller,
J. Nat. Prod. 2017, 80, 983-988.

266. A ligand-directed divergent catalytic approach to establish structural and functional scaffold diversity:
Y.-C. Lee, S. Patil, C. Golz, C. Strohmann, S. Ziegler, K. Kumar, H. Waldmann,
Nature Commun. 2017, 8, 14043-14054.

265. Solid State bonding situation of benzyl silanes: Influence of an intramolecular ammonium group:
F. Otte, S.G. Koller, E. Cuellar, C. Golz, C. Strohmann,
Inorg. Chim. Acta 2017, 456, 44-48.

264. Syntheses, solid structures, and behavior in solution of [MI2(CO)3(pyrazole)2] complexes (M = Mo, W):
P. Paredes, F. Lorenzo, S. Bajo, E. Cuéllar, C. Strohmann, J. M. Martín-Alvarez, D. Miguel, F. Villafañe,
Inorg. Chim. Acta 2017, 456, 9-17.

263. Secondary metabolites from Aspergillus japonicus CAM231, an endophytic fungus associated with Garcinia preussii:
J.-B. Jouda, J.-L. D. Fopossi, F. M. Kengne, C. Djama Mbazoa, C. Golz, C. Strohmann, S. K. Fogue, J. Wandji,
Nat. Prod. Res. 2017, 31, 861-869.

262. Biology-Oriented Synthesis of 3,3-Spiro(2-tetrahydrofuranyl)oxindoles:
S. Murarka, C. Golz, C. Strohmann, A.P. Antonchick, H. Waldmann,
Synthesis 2017, 49, 87-95.

261. Silver(I)-Catalyzed Enantioselective [3+2]-Cycloaddition Reaction of α-Silylimines: A Facile Route to Quaternary-Carbon Rich Scaffolds:
N. Kesava-Reddy, C. Golz, C. Strohmann, K. Kumar,
Chem. Eur. J. 2016, 22, 18373-18377.

260. Crystal structures of diaquadi-µ-hydroxido-tris[trimethyltin(IV)] diformatotrimethylstannate(IV) and di-µ-hydroxido-tris[trimethyltin(IV)] chloride monohydrate:
F. Otte, S.G. Koller, C. Golz, C. Strohmann,
Acta Cryst. E 2016, 72, 1499-1502.

259. The 3D [(Cu2Br2){μ-EtS(CH2)4SEt}]n Material: A Rare Example of a Coordination Polymer Exhibiting Triplet-Triplet Annihilation:
P.D Harvey, A. Bonnot, P.-L. Karsenti, F. Juvenal, C. Golz, C. Strohmann, D. Fortin, M. Knorr,
Phys. Chem. Chem. Phys., 2016, 18, 24845-24849.

258. Synthesis of an Iridoid-Inspired Compound Collection and Discovery of Autophagy Inhibitors:
P. Schröder, J.O. Bauer, C. Strohmann, K. Kumar, H. Waldmann,
J. Org. Chem. 2016, 81, 10242-10255.

257. Engaging Allene-Derived Zwitterions in an Unprecedented Mode of Asymmetric [3+2]-Annulation Reaction:x
M.G. Sankar, M. Garcia-Castro, C. Golz, C. Strohmann, K. Kumar,
Angew. Chem. Int. Ed. 2016, 55, 9709-9713.

256. L-Isoleucine derived bifunctional phosphine catalyses asymmetric [3 + 2]-annulation of allenyl-esters and -ketones with ketimines:
M.G. Sankar, M. Garcia-Castro, C. Golz, C. Strohmann, K. Kumar,
RSC Adv. 2016, 6, 56537-56543.

255. Three Cyclic Pentapeptides and a Cyclic Lipopeptide Produced by Endophytic Fusarium decemcellulare LG53:
G. Li, S. Kusari, C. Golz, C. Strohmann, M. Spiteller,
RSC Adv. 2016, 6, 54092-54098.

254. Enantiodivergent Combination of Natural Product Scaffolds Enabled by Catalytic Enantioselective Cycloaddition:
H. Xu, C. Golz, C. Strohmann, A.P. Antonchick, H. Waldmann,
Angew. Chem. Int. Ed. 2016, 55, 7761-7765.

253. Asymmetric Roadmap to Diverse Polycyclic Benzopyrans via Phosphine-Catalyzed Enantioselective [4+2]-Annulation Reaction:
A. Danda, N. Kesava-Reddy, C. Golz, C. Strohmann, K. Kumar,
Org. Lett. 2016, 18, 2632-2635.

252. (4S,5S,6R,E)-3,5-Dimethyl-6-vinylhept-2-ene-1,4,7-triol:
V. von Kiedrowski, F. Quentin, C. Golz, C. Strohmann, H. Preut, M. Hiersemann,
IUCrData 2016, 1, x160697.

251. Stoichiometry-controlled cycloaddition of nitrilimines with unsymmetrical exocyclic dienones: Microwave-assisted synthesis of novel mono and dispiropyrazoline derivatives:
H. Gazzeh, S. Boudriga, M. Askri, A. Khatyr, M. Knorr, C. Strohmann, C. Golz, Y. Rousselin, M.M. Kubicki,
RSC Adv. 2016, 6, 49868-49875.

250. Recent Progress in Asymmetric Synthesis and Application of Difunctionalized Silicon-Stereogenic Silanes:
J.O. Bauer, C. Strohmann,
Eur. J. Inorg. Chem. 2016, 2868-2881.

249. Antibacterial Azaphilones from an Endophytic Fungus Colletotrichum sp. BS4:
W.-X.Wang, S. Kusari, H. Laatsch, C. Golz, P. Kusari, C. Strohmann, O. Kayser, M. Spiteller,
J. Nat. Prod. 2016, 79, 704-710.

248. 1,4-Bis(arylthio)but-2-enes as Assembling Ligands for (Cu2X2)n (X= I, Br; n = 1, 2) Coordination Polymers: Aryl Substitution, Olefin Configuration, and Halide Effects on the Dimensionality, Cluster Size, and Luminescence Properties:
A. Bonnot, M. Knorr, F. Guyon, M. Kubicki, Y. Rousselin, C. Strohmann, D. Fortin, P. Harvey,
Crystal Growth & Design 2016, 16, 774-788.

247. Crystal structure of N′-[(E)-(1S,3R)-(3-isopropyl-1-methyl-2-oxocyclopentyl)methylidene]-4- methylbenzenesulfonohydrazide:
D. Tymann, D.C. Dragon, C. Golz, H. Preut, C. Strohmann, M. Hiersemann,
Acta Cryst. E 2015, 71, o904-o905.

246. Crystal structure of di-μ-iodido-bis{[bis(piperidin-1-yl)methane-κ2N,N’]copper(I)}:
E.R. Barth, C. Golz, C. Strohmann,
Acta Cryst. E 2015, 71, m193-m194.

245. Crystal structure of di-μ-iodido-bis[bis(acetonitrile-κN)copper(I)]:
E.R. Barth, C. Golz, M. Knorr, C. Strohmann,
Acta Cryst. E 201571, m189-m190.

244. Crystal structure of benzyl(methyl)phenyl[(piperidin-1-ium-1-yl)methyl]silane bromide:
E.R. Barth, C. Golz, S.G. Koller, C. Strohmann,
Acta Cryst. E 2015, 71, o759.

243. Crystal structure of borated N,N,N',N'-tetramethyldiaminomethane:
K. Louven, G. Quentin, C. Strohmann,
Acta Cryst. E 2015, 71, o743-o744.

242. Crystal structure of rac-(3aR,4S,5aR,6S,9R,10aS,10bR)-3a,5a,9-trimethyltetradecahydro-6,9-epoxycyclohepta[e ]inden-4-ol monohydrate:
A. Schäfer, C. Golz, H. Preut, C. Strohmann, M. Hiersemann,
Acta Cryst. E 2015, 71, o690-o691.

241. Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction:
S. Haddad, S. Boudriga, F. Porzio, A. Soldera, M. Askri, M. Knorr, Y. Rousselin, M. Kubicki, C. Golz, C. Strohmann,
J. Org. Chem. 2015, 80, 9064-9075.

240. Design of novel dispirooxindolopyrrolidine and dispirooxindolopyrrolothiazole derivatives as potential antitubercular agents:
C. Mhiri, S. Boudriga, M. Askri, M. Knorr, D. Sriram, P. Yogeeswari, F. Nana, C. Golz, C. Strohmann,
Bioorg. Med. Chem. Lett. 2015, 25, 4308-4313.

239. Hydrogen Bonding Principles in Inclusion Compounds of Triphenylsilanol and Pyrrolidine: Synthesis and Structural Features of [(Ph3SiOH)4·HN(CH2)4] and [Ph3SiOH·HN(CH2)4·CH3CO2H]:
J.O. Bauer, C. Strohmann,
J. Organomet. Chem. 2015, 797, 52-56.

238. Crystal structure of 4-(trimethylgermyl)benzoic acid:
L. Knauer, E.R. Barth, C. Golz, C. Strohmann,
Acta Cryst. E 2015, 71, 687-689.

237. Crystal structure of 1-[(2,4,6-triisopropylphenyl)sulfonyl]aziridine:
L. Knauer, C. Golz, C. Strohmann,
Acta Cryst. E 2015, 71, o438-o439.

236. Crystal structure of dibenzyldimethylsilane:
L. Knauer, C. Golz, U. Kroesen, S.G. Koller, C. Strohmann,
Acta Cryst. E 2015, 71, o391-o392.

235. Antiplasmodial and Cytotoxic Triterpenoids from the Bark of the Cameroonian Medicinal Plant Entandrophragma congoënse:
G.M. Happi, S.F. Kouam, F.M. Talontsi, M. Lamshöft, S. Zühlke, J.O. Bauer, C. Strohmann, M. Spiteller,
J. Nat. Prod. 2015, 78, 604-614.

234. Crystal structure of [2-(triethylammonio)ethyl]-[(2,4,6-triisopropylphenyl)sulfonyl]amide tetrahydrate:
C. Golz, C. Strohmann,
Acta Cryst. E 2015, 71, 564-566.

233. Stereocontrol in Nucleophilic Substitution Reactions at Silicon: The Role of Permutation in Generating Silicon-Centered Chirality:
J.O. Bauer, C. Strohmann,
J. Am. Chem. Soc. 2015, 137, 4304-4307.

232. Enantiogroup-differentiating biocatalytic reductions of prochiral Cs-symmetrical dicarbonyl compounds to meso compounds:
M. Skoupi, C. Vaxelaire, C. Strohmann, M. Christmann, C.M. Niemeyer,
Chem. Eur. J. 2015, 21, 8701-8705.

231. Design, synthesis and 3D-QSAR studies of novel 1,4-dihydropyridines as TGFβ/Smad signaling inhibitors:
D. Längle, V. Marquardt, E. Heider, B. Vigante, G. Duburs, I. Luntena, D. Flötgen, C. Golz, C. Strohmann, O. Koch, D. Schade,
Eur. J. Med. Chem. 2015, 95, 249-266.

230. Biology-Oriented Synthesis of a Withanolide-Inspired Compound Collection Reveals Novel Modulators of Hedgehog Signaling:
J. Švenda, M. Sheremet, L. Kremer, L. Maier, J.O. Bauer, C. Strohmann, S. Ziegler, K. Kumar, H. Waldmann,
Angew. Chem. 2015, 127, 5688-5694.

229. Reactivity of CuI and CuBr towards Dialkyl Sulfides RSR: From Discrete Molecular Cu4I4S4 and Cu8I8S6 Clusters to Luminescent Copper(I) Coordination Polymers:
M. Knorr, A. Bonnot, A. Lapprand, A. Khatyr, C. Strohmann, M. Kubicki, Y. Rousselin, P. Harvey,
Inorg. Chem. 2015, 54, 4076-4093.

228. Biology-Oriented Synthesis of Benzopyrano[3,4-c]pyrrolidines:
M. Potowski, C. Golz, C. Strohmann, A.P. Antonchick, H. Waldmann,
Bioorg. Med. Chem. 2015, 23, 2895-2903.

227. De novo branching cascades for structural and functional diversity in small molecules:
M. Garcia-Castro, L. Kremer, C.D. Reinkemeier, C. Unkelbach, C. Strohmann, S. Ziegler, C. Ostermann, K. Kumar,
Nature Commun. 2015, 6, 6516-6528.

226. Regioselective Annulation of Nitrosopyridine with Alkynes: Straightforward Synthesis of N-Oxide-imidazopyridines:
S. Manna, R. Narayan, C. Golz, C. Strohmann, A.P. Antonchick,
Chem. Commun. 2015, 51, 6119-6122.

225. CuX (X = Cl, Br, I) Containing Coordination Polymers Built Upon Isomeric RSCH2C≡CCH2SR (R = p-Tolyl, Benzyl) Dithioether Ligands: First Example of a Luminescent (CuCl)n/Dithioether Network:
A. Bonnot, M. Knorr, C. Strohmann, C. Golz, D. Fortin, P. Harvey,
J. Inorg. Organomet. Polymers and Materials 2015, 25, 480-494.

224. Stereoselective synthesis of a natural product inspired tetrahydroindolo[2,3-a]-quinolizine compound library:
M. G. Sankar, L. Mantilli, J. Bull, F. Giordanetto, J.O. Bauer, C. Strohmann, H. Waldmann, K. Kumar,
Bioorg. Med. Chem. 2015, 23, 2614-2620.

223. Synthesis and Reactivity of Bis(diphenylphosphino)amine-bridged Heterobimetallic Iron-Platinum μ-Isonitrile and μ-Aminocarbyne Complexes:
M. Knorr, I. Jourdain, A.S. Mohamed, A. Khatyr, S.G. Koller, C. Strohmann,
J. Organomet. Chem. 2015, 780, 70-85.

222. Oxidative regioselective amination of chromones exposes potent inhibitors of the hedgehog signaling pathway:
R. Samanta, R. Narayan, J.O. Bauer, C. Strohmann, S. Sievers, A.P. Antonchick,
Chem. Commun. 2015, 51, 925-928.

221. Crystal structure of (E)-N'-(((1R,3R)-3-isopropyl-1-methyl-2-oxocyclopentyl)methylene)-4-methylbenzenesulfonohydrazide:
D. Tymann, D.C. Dragon, C. Golz, H. Preut, C. Strohmann, M. Hiersemann,
Acta Cryst. E 2015, 71, o99-o100.

220. Coordination RC6H4S(CH2)8SC6H4R/(CuI)n Polymers (R (n) = H (4); Me (8)): An Innocent Methyl Group that Makes the Difference:
P.D. Harvey, A. Bonnot, A. Lapprand, C. Strohmann, M. Knorr,
Macromol. Rapid Commun. 2015, 36, 654-659.

219. A Route to Stereochemically Pure Benzyllithium Reagents by Stereocontrolled Epimerisation:x
S.G. Koller, U. Kroesen, C. Strohmann,
Chem. Eur. J. 2015, 21, 641-647.

218. Highly Enantioselective Intramolecular 1,3-Dipolar Cycloaddition: A Route to Piperidino-Pyrrolizidines:
S.R. Vidadala, C. Golz, C. Strohmann, C.G. Daniliuc, H. Waldmann,
Angew. Chem. Int. Ed. 2015, 54, 651-655.

217. Structural Consequences of an Extreme Difference between the Trans Influence of the Donor Atoms in a Palladacycle:
S.G. Koller, R. Martín-Romo, J. Melero, V. Colquhoun, D. Schildbach, C. Strohmann, F. Villafan~e,
Organometallics 2014, 33, 7329-7332.

216. Pyrazolylamidino Ligands from Coupling of Acetonitrile and Pyrazoles: A Systematic Study:
P. Go´mez-Iglesias, M. Arroyo, S. Bajo, C. Strohmann, D. Miguel, F. Villafan~e,
Inorg. Chem. 2014, 53, 12437-12448

215. Anellierte Diamine als nützliche Dikationen am Beispiel der Darstellung von Halocupratsalzen:
C. Golz, P. Eckert, C. Strohmann,
Z. Naturforsch. 2014, 69b, 1395-1401.

214. Copper(I) Halides (X = Br, I) Coordinated to Bis(arylthio)methane Ligands: Aryl Substitution and Halide Effects on the Dimensionality, Cluster Size, and Luminescence Properties of the Coordination Polymers:
M. Knorr, A. Khatyr, A.D. Aleo, A. El Yaagoubi, C. Strohmann, M.M. Kubicki, Y. Rousselin, S.M. Aly, D. Fortin, A. Lapprand, P.D. Harvey,
Cryst. Growth Des. 2014, 14, 5373-5387.

213. Indolosesquiterpene Alkaloids from the Cameroonian Medicinal Plant Polyalthia Oliveri (Annonaceae):
S.F. Kouam, A.W. Ngouonpe, M. Lamshöft, F.M. Talontsi, J.O. Bauer, C. Strohmann, B.T. Ngadjui, H. Laatsch, M. Spiteller,
Phytochem. 2014, 105, 52-59.

212. A Cyclization-Rearrangement Cascade for the Synthesis of Structurally Complex Chiral Gold(I)-Aminocarbene Complexes:
F. Kolundžic, A. Murali, P. Pérez-Galán, J.O. Bauer, C. Strohmann, K. Kumar, H. Waldmann,
Angew. Chem. 2014, 126, 8260-8264;
Angew. Chem. Int. Ed. 2014, 53, 8122-8126.

211. From an α-Functionalized Silicon-Stereogenic N,O-Silane to a Monomeric and Tetracoordinate tBuLi Adduct with Lithium-Centered Chirality:
J.O. Bauer, C. Strohmann,
Angew. Chem. 2014, 126, 8306-8310;
Angew. Chem. Int. Ed. 2014, 53, 8167-8171.

210. A Bioinspired Catalytic Oxygenase Cascade to Generate Complex Oxindoles:
Y. Wang, J.O. Bauer, C. Strohmann, K. Kumar,
Angew. Chem. 2014, 126, 7644-7648;
Angew. Chem. Int. Ed. 2014, 53, 7514-7518.

209. A Formal, One-Pot beta-Chlorination of Primary Alcohols and Its Utilization in the Transformation of Terpene Feedstock and the Synthesis of a C2-Symmetrical Terminal Bis-Epoxide:
J. Swatschek, L. Grothues, J.O. Bauer, C. Strohmann, M. Christmann,
J. Org. Chem. 2014, 79, 976-983.

208. Unexpected Structural Motifs in Diamine Coordination Compounds with Allyllithium:
P.K. Eckert, B. Schnura, C. Strohmann,
Chem. Commun. 2014, 50, 2532-2534.

207. (rac)-2-Phenyl-1-(2,4,6-triisopropylbenzenesulfonyl)aziridine:
C. Golz, H. Preut, C. Strohmann,
Acta Cryst. E 2014, 70, o153.

206. 1,3-Dipolar Cycloaddition Reactions of Indan-1-one Enamines across Arylnitrile Oxides Leading to Novel Cyclic Isoxazoline Derivatives:
H. Jelizi, N. Wannassi, M. El Baker Rammah, K. Ciamala, M. Knorr, Y. Rousselin, M.M. Kubicki, C. Strohmann, M. Enescue,
J. Het. Chem. 2014, 51, 383-391.

205. Exploring the Synthesis of a New Group of Chiral Ammonium Salts with Specific Configurations at the Stereogenic Nitrogen Centers:
P.K. Eckert, C. Golz, P. Degen, C. Werner, H. Rehage, C. Strohmann,
Chem. Eur. J. 2014, 20, 3268-3272.

204. Insights into the Metalation of Benzene and Toluene by Schlosser's Base: A Bimetallic, Superbasic Cluster comprising PhK, PhLi and tBuOLi:
C. Unkelbach, D.F. O'Shea, C. Strohmann,
Angew. Chem. Int. Ed. 201453, 553-556.

203. Stereoselective Synthesis of Silicon-Stereogenic Aminomethoxysilanes: Easy Access to Highly Enantiomerically Enriched Siloxanes:
J.O. Bauer, C. Strohmann,
Angew. Chem. 2014, 126, 738-742;
Angew. Chem. Int. Ed. 2014, 53, 720-724.

202. Cluster-containing Coordination Polymers Built Upon (Cu2I2S2)m Units (m = 2, 3) and ArSCH2C≡CCH2SAr Ligands; is the Cluster Size Dependent upon Steric Hindrance or Ligand Rigidity?:
S.M. Aly, A. Pam, A. Khatyr, M. Knorr, Y. Rousselin, M.M. Kubicki, J.O. Bauer, C. Strohmann, P.D. Harvey,
J. Inorg. Organomet. Polym. Mat. 2014, 24, 190-200.

201. Metal-to-Ligand Ratio Effect on the Size of Copper Iodide and Copper Bromide Clusters in 1,4-Bis(cyclohexylthio)butanespanned Coordination Polymers:
A. Bonnot, C. Strohmann, M. Knorr, P.D. Harvey,
J. Clust. Sci. 2014, 25, 261-275.

200. Catalytic Enantioselective Synthesis of Functionalized Tropanes Reveals Novel Inhibitors of Hedgehog Signaling:
R. Narayan, J.O. Bauer, C. Strohmann, A.P. Antonchick, H. Waldmann,
Angew. Chem. Int. Ed. 2013, 125, 13130-13134.

199. Discovery of Inhibitors of the Wnt and Hedgehog Signaling Pathway through the Catalytic Enantioselective Synthesis of an Iridoid-Inspired Compound Collection:
H. Takayama, Z.-J. Jia, L. Kremer, J.O. Bauer, C. Strohmann, S. Ziegler, A.P. Antonchick, H. Waldmann,
Angew. Chem. Int. Ed. 2013, 52, 12404-12408.

198. Reactivity of Silyl-substituted Iron-Platinum Hydride Complexes towards Unsaturated Molecules: Part IV. Insertion of Fluorinated Aromatic Alkynes into the Platinum-Hydride Bond. Synthesis and Reactivity of Heterobimetallic Dimetallacylopentenone, Dimetallacyclobutene, μ-Vinylidene and μ2-σ Alkenyl Complexes:
I. Jourdain, M. Knorr, C. Strohmann, C. Unkelbach, S. Rojo, P. Gómez-Iglesiasc, F. Villafañe,
Organometallics 2013, 32, 5343-5359.

197. Catalytic and Stereoselective ortho-Lithiation of a Ferrocene Derivative:
P. Steffen, C. Unkelbach, M. Christmann, W. Hiller, C. Strohmann,
Angew. Chem. Int. Ed. 2013, 52, 9836-9840.

196. Understanding Structure Formation in Organolithium Compounds: An Experimental and Quantum-Chemical Approach:
K. Götz, V.H. Gessner, C. Unkelbach, M. Kaupp, C. Strohmann,
Z. Anorg. Allg. Chem. 2013, 639, 2077-2085.+

195. Antibacterial and Antiplasmodial Constituents of Beilschmiedia cryptocaryoides:
F.M. Talontsi, M. Lamshöft, J.O. Bauer, A.A. Razakarivony, B. Andriamihaja, C. Strohmann, M. Spiteller,
J. Nat. Prod. 2013, 76, 97-102.

194. Reinvestigation of the Pd-Catalysed Bis(silylation) of Alkynes with 1,1,2,2-Tetramethyl-1,2-bis(phenylthiomethyl)disilane: Unexpected Formation of the Eight-Membered Siloxane-Chelate complex cis-[PdCl2{(PhSCH2SiMe2)2O}]:
H.W. Peindy N`dongo, S. Clément, S. Richeter, F. Guyon, M. Knorr, P. le Gendre, J.O. Bauer, C. Strohmann,
J. Organomet. Chem. 2013, 724, 262-270.

193. Simple is best: diamine zinc complexes as unexpected catalysts in lactide polymerisation:
P.K. Eckert, I. dos Santos Vieira, V.H. Gessner, J. Börner, C. Strohmann, S. Herres-Pawlis,
Polyhedron 2013, 49, 151-157.

192. Organocatalytic, Oxidative, Intermolecular Amination and Hydrazination of Simple Arenes at Ambient Temperature:
R. Samanta, J.O. Bauer, C. Strohmann, A.P. Antonchick,
Org. Lett. 2012, 14, 5518-5521.

191. Direct Benzylic Metalation of a Phenethylamine Derivative: Potassium as the Key to both Generation and Stabilization of a “Labile Anion”:
C. Unkelbach, H.S. Rosenbaum, C. Strohmann,
Chem. Commun. 2012, 48, 10612-10614.

190. Construction of (CuX)2n Cluster-Containing (X = Br, I; n = 1, 2) Coordination Polymers Assembled by Dithioethers ArS(CH2)mSAr (Ar = Ph, p‑Tol; m = 3, 5): Effect of the Spacer Length, Aryl Group, and Metal-to-Ligand Ratio on the Dimensionality, Cluster Nuclearity, and the Luminescence Properties of the Metal−Organic Frameworks:
M. Knorr, F. Guyon, A. Khatyr, C. Strohmann, M. Allain, S.M. Aly, A. Lapprand, D. Fortin, P.D. Harvey,
Inorg. Chem. 2012, 51, 9917-9934.

189. Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides:
M. Potowski, J.O. Bauer, C. Strohmann, A.P. Antonchick, H. Waldmann,
Angew. Chem. 2012, 124, 9650-9654.

188. Formation of Specific Configurations at Stereogenic Nitrogen Centers upon their Coordination to Zinc and Mercury:
P.K. Eckert, V.H. Gessner, M. Knorr, C. Strohmann,
Inorg. Chem. 2012, 51, 8516-8523.

187. Metal-Free Electrocyclization at Ambient Temperature: Synthesis of 1-Aryl-carbazoles:
R. Samanta, K. Kulikov, C. Strohmann, A.P. Antonchick,
Synthesis 2012, 44, 2325-2332.

186. One-Step Conversion of Methoxysilanes to Aminosilanes: A Convenient Synthetic Strategy to N,O-Functionalised Organosilanes:
J.O. Bauer, C. Strohmann,
Chem. Commun. 2012, 48, 7212-7214.

185. {4-t-Bu-2,6-[P(O)(O-i-Pr)2]2C6H2Sn}2: An Intramolecularly Coordinated Organo-tin(I) Compound with a Sn–Sn Single Bond, Its Disproportionation toward a Diorganostannylene and Elemental Tin, and Its Oxidation with PhI(OAc)2:
M. Wagner, C. Dietz, S. Krabbe, S.G. Koller, C. Strohmann, K. Jurkschat,
Inorg. Chem. 2012, 51, 6851-6859.

184. Palladium(II)-Catalyzed Cycloisomerization of Substituted 1,5-Hexadienes: A Combined Experimental and Computational Study on an Open and an Interrupted Hydropalladation /Carbopalladation/β-Hydride Elimination (HCHe) Catalytic Cycle:x
B. Nelson, S. Herres-Pawlis, W. Hiller, H. Preut, C. Strohmann, M. Hiersemann,
J. Org. Chem. 2012, 11, 4980-4995.

183. Syntheses, Dynamic Behaviour and Theoretical Studies of (Piperidinomethyl)silylmethyl Cyclopalladated Bimetallic Complexes:
V.P. Colquhoun, D. Schildbach, R. Martín-Romo, C. Strohmann, F. Villafañe,
Eur. J. Inorg. Chem. 2012, 3427-3434.

182. 4,5-Bis(methylthio)-1,3-dithiole-2-thione, a versatile sulphur-rich building block 3 for the self-assembly of Cu(I) and Ag(I) coordination polymers: Dithioether versus 4 thiocarbonyl bonding:
A. Hameau, F. Guyon, A. Khatyr, M. Knorr, C. Strohmann,
Inorg. Chim. Acta 2012, 388, 60-70.

181. Bridging Pseudohalides in Palladacycles as Source of different Assemblies:
M. Arroyo, P. Gómez-Iglesias, J. Santos Melero, D. Schildbach, C. Unkelbach, C. Strohmann, F. Villafañe,
Eur. J. Inorg. Chem. 2012, 3302-3307.

180. 1,3-Dipolar cycloaddition reactions of indan-1-one enamines across arylnitrile oxides leading to novel cyclic isoxazoline derivatives:
N. Wannassi, H. Jelizi, M. El Baker Rammah, K. Ciamala, M. Knorr, K. Monnier-Jobé, Y. Rousselin, M.M. Kubicki, C. Strohmann,
Heterocycles 2012, 85, 835-849.

179. Isolation of reactive intermediates in deprotonation reactions with zinc alkyls:
V.P. Colquhoun, C. Unkelbach, C. Strohmann,
Chem. Commun. 2012, 48, 5034-5036.

178. Platinum(II) complexes bearing thiolate/thioether ligand: hemilability versus dealkylation:
F. Guyon, M. Knorr, A. Garillon, C. Strohmann,
Eur. J. Inorg. Chem. 2012, 2012, 282-291.

177. Triphen-yl(prop-2-yn-1-yl)silane:
B. Nelson, M. Schulte, C. Strohmann, H. Preut, M. Hiersemann,
Acta Cryst. E 2012, 68, o452.

176. Preparation of Aminomethyl Functionalised Silanes via an α-lithiated Amine: From their Synthesis, Stability and Crystal Structures to Stereochemical Issues:
V.H. Gessner, C. Strohmann,
Dalton Trans. 2012, 41, 3452-3460.

175.  A Diastereomerically Enriched, Dimeric Organolithium Compound and the Stereochemical Course of its Transformations:
C. Unkelbach, B.C. Abele, K. Lehmen, D. Schildbach, B. Waerder, K. Wild, C. Strohmann,
Chem. Commun. 2012, 48, 2492-2494.

174. Structural Influence of Steric Factors and Donor Functions on Lithium Silylamides in Non-coordinating Solvents:
V.P. Colquhoun, C. Strohmann,
Dalton Trans. 2012, 41, 1897-1902.

173. [μ-Bis(diphenyl-phosphan-yl))methane]-tricarbon-yl(μ-p-toluene-sulfonyl-meth-yl-isocyanato)(triphenyl-phosphane)ironplatinun(Fe-Pt):
I. Jourdain, M. Knorr, S.G. Koller, C. Strohmann,
Acta Cryst. E  2012, 68, m331-m332.

172. Synthesis, crystallographic and electrochemical study of ethynyl[2.2]paracyclophane derived cobalt metallatetrahedranes:
S. Clément, L. Guyard, A. Khatyr, M. Knorr, Y. Rousselin, M.M. Kubicki, Y. Mugnier, S. Richeter, P. Gerbier, C. Strohmann,
J. Organomet. Chem. 2012, 699, 56-66.

171. (4R)-4-Benzyl-3-{(4S)-4-chloro-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]butanoyl}-1,3-oxazolidin-2-one:
S. Boerding, C. Strohmann, H. Preut, M. Hiersemann,
Acta Cryst. E 2012, 68, o169.

 

170. Theoretical and sprectroscopic studies on the conformational equilibrium of 9-oxabi-spidines in solution:
M. Breuning, A. Paasche, M. Steiner, S. Dilsky, V.H. Gessner, C. Strohmann, B. Engels,
J. Mol. Struc. 2011, 1005, 178-185.

169. 1-Phenyl-5-{[2-(trimethylsilyl)ethyl]-sulfonyl}-1H-tetrazole:
D. Tymann, B. Nelson, C. Strohmann, H. Preut, M. Hiersemann,
Acta Cryst. E  2011, 67, o2369.

168. Total Synthesis and Biological Evaluation of (−)-Englerin A and B: Synthesis of Analogues with Improved Activity Profile:
L. Radtke, M. Willot, H. Sun, S. Ziegler, S. Sauerland, C. Strohmann, R. Fröhlich, P. Habenberger, H. Waldmann, M. Christmann,
Angew. Chem. 2011, 123, 4084-4088.

167. Mechanistic Insight into Stereoselective Carbolithiation:
V.H. Gessner, S.G. Koller, C. Strohmann, A.-M.L. Hogan, D.F. O’Shea,
Chem. Eur. J. 2011, 17, 2996-3004.

166. Control of N- or C-bridging Mode in Dimeric Butylmagnesium Silylamides:
V.P. Colquhoun, B.C. Abele, C. Strohmann,
Organometallics 2011, 30, 5408-5414.

165. Synthesis of cis-TMCDA: Optimization and characterization of a key intermediate:
P.K. Eckert, V. Schill, C. Strohmann,
Inorg. Chim. Acta 2011, 376, 634-637.

164. Two-dimensional polymeric [Hg4(µ2-I)6I2(µ2-C4S6)]n:
A. Hameau, F. Guyon, M. Knorr, V.P. Colquhoun, C. Strohmann,
Acta Cryst. E  2011, 67, m389.

163. 2-(2’,2’-Dibromoethenyl)thiophene:
S. Clément, L. Guyard,  M. Knorr, P.K. Eckert, C. Strohmann,
Acta Cryst. E  2011, 67, o481.

162. Enantioselective α- and γ-Alkylation of α,β-Unsaturated Aldehydes Using Dienamine Activation:
J. Stiller, E. Marques-Lopez, R.P. Herrera, R. Frohlich, C. Strohmann, M. Christmann,
Org. Lett. 2011, 13, 70-73.

161. Mechanistic insights into the Reaction of Enantiomerically Pure Lithiosilanes and Electrophiles: Understanding the Differences between Aryl- and Alkyl Halides:
C. Däschlein, S.O. Bauer, C. Strohmann,
Eur. J. Inorg. Chem. 2011, 9, 1454-1465.

160. Process for Catalytic ring-opening polymerization of cyclic monomers:
C. Strohmann, S. Herres-Pawlis, V.H. Gessner, J. Boerner, P. Eckert, K. Jurkschat, G. Bradtmoeller, M. Schuermann, M. Gock,
PCT Int. Appl.

159. Catalytic ring-opening polymerization of cyclic monomers:
C. Strohmann, S. Herres-Pawlis, V.H. Gessner, J. Boerner, P. Eckert,
Ger. Offen.

158. Stereogenic nitrogen centers with specific configuration: Coordination of chiral diamines to transition metals:
P.K. Eckert, G. Dropalla, V.H. Gessner, C. Strohmann,
Abstracts of Papers, 240th ACS National Meeting 2010, INOR-199.

157. Silyl-Modified Analogues of 2-Tritylpyrrolidine: Synthesis and Applications in Asymmetric Organocatalysis:
J.O. Bauer, J. Stiller, E. Marqués-López, K. Strohfeldt, M. Christmann, C. Strohmann,
Chem. Eur. J. 2010, 16, 12553-12558.

156. α-Lithiated (R,R)-TMCDA as Efficient Building Block for the Preparation of Chiral N,N,O-Ligands via Asymmetric 1,2-Addition:
V.H. Gessner, B. Fröhlich, C. Strohmann,
Eur. J. Inorg. Chem., 2010, 36, 5640-5649.

155. {2,2-Bis[(4S)-4-isopropyl-4,5-dihydro-1,3-oxazol-2-yl]propane}bis(N,N-dimethylfor-mamide)copper(II) bis[hexafluoridoantimonate(V)]:
J. Zeh, M. Moeller, C. Strohmann, H. Preut, M. Hiersemann,
Acta Cryst. E  2010, 66, m1688.

154. Synthesis of P-Stereogenic Compounds via Kinetic Deprotonation and Dynamic Thermodynamic Resolution of Phosphine Sulfides: Opposite Sense of Induction Using (-)-Sparteine:
J.J. Gammon, V.H. Gessner, G.R. Barker, J. Granander, A.C. Whitwood, C. Strohmann, P. O’Brien, B. Kelly,
J. Am. Chem. Soc. 2010, 132, 13922-13927.

153. Lithiumorganyle: Zwischen Ästhetik und Verständnis:
V.H. Gessner, C. Strohmann,
Nachr. Chem. Tech. Lab. 2010, 58, 744-747.

152. Unexpected Direct Dilithiation of a Prochiral Phosphino Borane:
V.H. Gessner, S. Dilsky, C. Strohmann,
Chem. Commun. 2010, 46, 4719-4721.

151. Reactivity of CuI and CuBr toward Et2S. A Reinvestigation on the Self-Assembly of Luminescent Copper(I) Coordination Polymers:
M. Knorr, F. Pam, A. Khatyr, C. Strohmann, M.M. Kubicki, Y. Rousselin, S.M. Aly, D. Fortin, P.D. Harvey,
Inorg. Chem. 2010, 49, 5834-5844.

150. Lithiation of Diamine Ligands to Chiral Building Blocks: Syntheses, Selectivities, and Lithiated Intermediates:
V.H. Gessner, C. Strohmann,
Organometallics 2010, 29, 1858-1861.

149. [{2,6-(Me2NCH2)2C6H3(H2O)Sn}W(CO)5]+CB11H12-: Aqua-complex of a transition-metal-bound organotin(II) cation versus an ammonium-type structure:
R. Jambor, B. Kašná, S.G. Koller, C. Strohmann, M. Schürmann, K. Jurkschat,
Eur. J. Inorg. Chem. 2010, 902-908.

148. tert-Butoxytriphenylsilane:
J.O. Bauer, C. Strohmann,
Acta Cryst. E 2010, 66, o461-o462.

147. The Competition Between Si–Si and Si–C Cleavage in Functionalised Oligosilanes: Their Reactivity with Elemental Lithium:
C. Däschlein, C. Strohmann,
Dalton Trans. 2010, 39, 2062-2069.

146. Preparation of ”Si-centred” Chiral Silanes by Direct α-Lithiation of Methylsilanes:
C. Däschlein, V.H. Gessner, C. Strohmann,
Chem. Eur. J. 2010, 16, 4048-4062.

145. Low-Temperature Addition of Organolithiums to Functionalized Vinylsilanes under Formation of Secondary α-Lithiated Alkylsilanes:
C. Unkelbach, C. Strohmann,
J. Am. Chem. Soc. 2009, 131, 17044-17045.

144. Selective Si–O–Si Bond cleavage as Synthetic Access to functionalized, hydrolysis- stable Zinc Silanolates:
C. Däschlein, C. Strohmann,
Z. Naturforsch. 2009, 64b, 1558-1566.

143. Totalsynthese und absolute Konfiguration des Guaian-Sesquiterpens Englerin A:
M. Willot, L. Radtke, D. Könning, R. Fröhlich, V.H. Gessner, C. Strohmann, M. Christmann,
Angew. Chem. 2009, 121, 9269-9272.

142. Enantioselective Synthesis of Tricyclic Amino Acid Derivatives Based on a Rigid 4-Azatricyclo[5.2.1.02,6]decane Skeleton:
M. Breuning, T. Häuser, C. Mehler, C. Däschlein, C. Strohmann, A. Oechsner, H. Braunschweig,
B. J. Org. Chem. 2009, 5, No. 81.

141. Diastereoselective synthesis and structure of spiroisoxazoline derivatives:
S. Boudriga, N. Wannassi, M. Askri, M. El Baker Rammah, C. Strohmann,
J. Soc. Chim. Tunisie 2009, 11, 29-36.

140. Synthesis of heterocyclic compounds of the arylnaphthaleno[1,2-d]isoxazole type by 1,3-dipolar cycloaddition of arylnitrile oxides on α-tetralone enamines:
I. Garrouch, M.M. Rammah, M. Askri, M.B. Rammah, M. Knorr, C. Strohmann,
J. Soc. Chim. Tunisie 2009, 11, 21-27.

139. Chiral 2-Endo-Substituted 9-Oxabispidines: Novel Ligands for Enantioselective Copper(II)-Catalyzed Henry Reactions:
M. Breuning, D. Hein, M. Steiner, V.H. Gessner, C. Strohmann,
Chem. Eur. J. 2009, 15, 12764-12769.

138. A Convenient Synthesis of Novel Spiroisoindolone γ-Halobutyrolactones via Halocyclization of γ-Ethylenic Acids:
M.M. Rammah, M. Othman, K. Ciamala, M. Knorr, C. Strohmann, M.B. Rammah,
Heterocycles 2009, 78, 2787-2798.

137. From the Selective Cleavage of the Si–O–Si Bond in Disiloxanes to Zwitterionic, Water-Stable Zinc-Silanolates:
C. Däschlein, J.O. Bauer, C. Strohmann,
Angew. Chem. 2009, 121, 8218–8221.

136. Dibromido[(tert-butylamino)dimethyl(piperidin-1-ylmethyl)silane-K2N,N’]zinc(II):
V.P. Colquhoun, C. Strohmann,
Acta Cryst. E 2009, 65, m680.

135. A-Frame-Containing Organometallic Oligomers Constructed from Homo- and Heterobimetallic M(µ-dppm)2M’ (M/M’ = Pd, Pt) Building Blocks:
S. Clement, S.M. Aly, J. Husson, D. Fortin, C. Strohmann, M. Knorr, L. Guyard, A.S. Abd-El-Aziz, P.D. Harvey,
Eur. J. Inorg. Chem. 2009, 2536-2546.

134. (1R,2R)-N,N'-Diisobutyl-N,N'-dimethylcyclohexane-1,2-diamine:
P.K. Eckert, V.H. Gessner, C. Strohmann,
Acta Cryst. E 2009, 65, o956.

133. Synthesis of diversely functionalized pyrrolizidines and indolizidines using olefin ring-closing metathesis:
R. Ben-Othman, M. Othman, K. Ciamala, M. Knorr, C. Strohmann, B. Decroix,
Tetrahedron 2009, 65, 4846-4854.

132. Properties of the [M(dppm)2M’]2+ Building Blocks (M, M’ = Pd or Pt) : Site Selectivity, Emission Features, and Frontier Orbital Analysis:
S. Clement, S.M. Aly, D. Bellows, D. Fortin, C. Strohmann, L. Guyard, A.S. Abd-El-Aziz, M. Knorr, P.D. Harvey,
Inorg. Chem. 2009, 48, 4118-4133.

131. Structure Formation Principles and Reactivity of Organolithium Compounds:
V.H. Gessner, C. Däschlein, C. Strohmann,
Chem. Eur. J. 2009, 15, 3320-3334.

130. Formation of Extended 1D and 2D Coordination Polymers in Tetrathioether Complexes of Mercury(II) and Copper(I): Crystal Structures of [{{Ge(CH2SPh)4}HgBr2}n] and [{{Ge(CH2SPh)4}(Cu2l2)}n]:
H.N. Peindy, F. Guyon, A. Khatyr, M. Knorr, V.H. Gessner, C. Strohmann,
Z. Anorg. Allg. Chem. 2009, 635, 2099-2105.

129. Selective Vinyl C-H Lithiation of cis-Stilbenes:
T. Tricotet, P. Fleming, J. Cotter, A.-M.L. Hogan, C. Strohmann, V.H. Gessner, D.F. O’Shea,
J. Am. Chem. Soc. 2009, 131, 3142-3143.

128. 2-[(2-Hydroxy-2,2-diphenylethyl)(methyl)amino]-N,N-dimethylethanaminium bromide:
V.H. Gessner, C. Däschlein, C. Strohmann,
Acta Cryst. E 2009, 65, o383.

127. 4,12-Bis(2,2-Dibromovinyl)[2.2]paracyclophane:
S. Clement, L. Guyard, M. Knorr, C. Däschlein, C. Strohmann,
Acta Cryst. E 2009, 65, o528.

126. (2,2-Dichlorovinyl)ferrocene:
S. Clement, L. Guyard, M. Knorr, V.H. Gessner, C. Strohmann,
Acta Cryst. E 2009, 65, m334.

125. Structural Studies on (–)-Sparteine Coordinated Lithiosilanes:
C.Däschlein, C. Strohmann,
Eur. J. Inorg. Chem. 2009, 43-52.

124. Rigidity Effect of the Dithioether Spacer on the Size of the Luminescent Cluster (Cu2I2)n (n = 2, 3) in their Coordination Polymers:
M. Knorr, F. Guyon, A. Khatyr, C. Däschlein, C. Strohmann, S.M. Aly, A.S. Abd-El-Aziz, D. Fortin, P.D. Harvey,
Dalton Trans. 2009, 948-955.

123. Lithiation of TMEDA and its Higher Homologous TEEDA: Understanding Observed α- and β-Deprotonation:
V.H. Gessner, C. Strohmann,
J. Am. Chem. Soc. 2008, 130, 14412-14413.

122. A precoordination complex of 1,2,3-trimethyl-1,3,5-triazacyclohexane with tert-buthyllithium as key intermediate in its methylene group deprotonation:
C. Strohmann, V.H. Gessner,
Chem. Asian J. 2008, 3, 1929-1934.

121. Isopropyllithium Diamine Adducts: From a Non Symmetric Aggregate to Monomeric i-PrLi·(1R,2R)-N,N,N',N'-Tetraethylcyclohexane-1,2-diamine:
C. Strohmann, V.H. Gessner, A. Damme,
Chem. Commun. 2008, 3381-3383.

120. Structure/Reactivity Studies on an α-Lithiated Benzylsilane: Chemical Interpretation of Experimental Charge Density:
H. Ott, C. Däschlein, D. Leusser, D. Schildbach, T. Seibel, D. Stalke, C. Strohmann,
J. Am. Chem. Soc. 2008, 130, 11901-11911.

119. Bent Phenyl Groups in Lithiosilanes – Crystal Structures and Interpretation of this Unanticipated Feature:
C. Strohmann, C. Däschlein,
Chem. Commun. 2008, 2791-2793.

118. (S)-1,2-Dimethyl-1,1,2-triphenyl-2-(4-piperidiniomethyl)disilane chloride:
C. Däschlein, V.H. Gessner, C. Strohmann,
Acta Cryst. E 2008, 64, o1950.

117. (1R,2R)-N,N'-Dimethylcyclohexane-1,2-diamine:
C. Strohmann, V.H. Gessner, A. Damme, S. Koller, C. Däschlein,
Acta Cryst. E 2008, 64, o687.

116. Synthesis and Reactivity of Silylated Tetrathiafulvalenes:
A. Hameau, F. Guyon, M. Knorr, C. Däschlein, C. Strohmann, N. Avarvari,
Dalton Trans. 2008, 4866-4876.

115. Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene:
C. Strohmann, V.H. Gessner,
J. Am. Chem. Soc. 2008, 130, 11719-11725.

114. Syntheses, Structures, and Photophysical Properties of Mono- and Dinuclear Sulfur-Rich Gold(I) Complexes:
F. Guyon, A. Hameau, A. Khatyr, M. Knorr, H. Amrouche, D. Fortin, P.D. Harvey, C. Strohmann, A.L. Ndiaye, V. Huch, M. Veith, N. Avarvari,
Inorg. Chem. 2008, 47, 7483-7492.

113. Synthesis of a Highly Enantiomerically Enriched Silagermane and Selective Cleavage of the Si–Ge Bond with Lithium:
C. Strohmann, C. Däschlein,
Organometallics 2008, 27, 2499-2504.

112. Silver-Catalyzed Spirolactonization: First Synthesis of Spiroisoindole-γ-Methylene-γ-Butyrolactones:
M.M. Rammah, M. Othman, K. Ciamala, C. Strohmann, M.B. Rammah,
Tetrahedron 2008, 64, 3505-3516.

111. Von monomerem tBuLi·(R,R)-TMCDA zu α-lithiiertem (R,R)-TMCDA:
C. Strohmann, V.H. Gessner,
Angew. Chem. 2007, 119, 8429-8432.

110. Crystal Structures of the Chiral Diamine (R,R)-TMCDA with the Commonly Used Alkyllithium Bases Methyllithium, iso-Propyllithium and sec-Butyllithium:
C. Strohmann, V.H. Gessner,
J. Am. Chem. Soc. 2007, 129, 8952-8953.

109. Von dem Alkyllithium-Aggregat [(n-BuLi)2·PMDTA]2 zu lithiiertem PMDTA:
C. Strohmann, V.H. Gessner,
Angew. Chem. 2007, 119, 4650-4653.

108. Ein hoch enantiomerenangereichertes Lithiosilan durch selektive Spaltung einer Silicium-Phenyl-Bindung mit Lithium:
C. Strohmann, C. Däschlein, M. Kellert, D. Auer,
Angew. Chem. 2007, 119, 4864-4866.

107. (2,2-Dibromovinyl)ferrocene as a building block for the assembly of heterodinuclear complexes – Preparation of an σ-alkenylpalladium complex and dimetallic dithioether complexes:
S. Clement, L. Guyard, M. Knorr, F. Villafañe, C. Strohmann, M.M. Kubicki,
Eur. J. Inorg. Chem. 2007, 5052-5061.

106. {[(C7H7LiO)6·(thf)2·(µ-diglyme-kO,kO')]Li2O}: a µ6-O2- ion encapsulating aryllithium compound:
C. Strohmann, V.H. Gessner,
Z. Anorg. Allg. Chem. 2007, 633, 2285-2287.

105. Ethynyl[2.2]paracyclophanes and 4-isocyano[2.2]paracyclophanes as ligands in organometallic chemistry:
S. Clément, L. Guyard, M. Knorr, S. Dilsky, C. Strohmann, M. Arroyo,
J. Organomet. Chem. 2007, 692, 839-850.

104. Synthesis of Some Spirochroman-4-Ones by Regioselective [4+2] Cycloaddition Reactions:
M. Askri, M. Rammah, K. Monnier-Jobé, K. Ciamala, M. Knorr, C. Strohmann,
Lett. Org. Chem. 2007, 4, 222-227.

103. Construction of 1D and 2D Copper(I) Coordination Polymers Assembled by PhS(CH2)nSPh (n = 1, 2) Dithioether Ligands: Surprising Effect of the Spacer Length on the Dimensionality, ClusterNuclearity and the Fluorescence Properties of the Metal-organic Framework:
H.N. Peindy, F. Guyon, A. Khatyr, M. Knorr, C. Strohmann,
Eur. J. Inorg. Chem. 2007, 1823-1828.

102. A Monolithiated and Its Related 1,3-Dilithiated Allylsilane: Syntheses, Crystal Structures, and Reactivity:
C. Strohmann, K. Lehmen, S. Dilsky,
J. Am. Chem. Soc., 2006, 128, 8102-8103.

101. Insertion Reactions of Alkynes and Organic Isocyanides into the Palladium-Carbon Bond of Dimetallic Fe-Pd Alkoxysilyl Complexes:
M. Knorr, I. Jourdain, P. Braunstein, C. Strohmann, A. Tiripicchio, F. Ugozzoli,
Dalton Trans. 2006, 5248-5258.

100. Crystal Structures of the Chiral Lithiosilanes [(Lis)-PhMe2SiLi·THF·(–)-Sparteine] and [Ph2(NEt2)SiLi·(–)-Sparteine]:
C. Strohmann, C. Däschlein, D. Auer,
J. Am. Chem. Soc. 2006, 128, 704-705.

99. Self-assembly of Dithiolene-based Coordination Polymers of Mercury(II). Dithioether versus Thiocarbonyl bonding:
A. Hameau, F. Guyon, M. Knorr, M. Enescu, C. Strohmann,
Monatsh. Chem. 2006, 137, 545-555.

98. Crystal Structures of [PhLi·(-)-sparteine]2, [PhOLi·(-)-sparteine]2 and the Mixed Aggregate [PhLi·PhOLi·2 (-)-sparteine]:
C. Strohmann, S. Dilsky, K. Strohfeldt,
Organometallics 2006, 25, 41-44.

97. Reactivity of silyl-substituted heterobimetallic iron-platinum hydride complexes: Part III. Alkyne insertions into the platinum-hydride bond and competition between µ-vinylidene and dimetallacyclopentenone formation:
I. Jourdain, L. Vieille-Petit, S. Clement, M. Knorr, F. Villafañe, C. Strohmann,
Inorg. Chem. Commun. 2006, 9, 127-131.

96. 1,1,2,2-Tetramethyl-1,2-bis(phenylthiomethyl)disilane, a Flexible Ligand for the Construction of Macrocyclic, Mesocyclic and Bridged Dithioether Complexes. Synthesis of the Bis-silylated Olefins Z-(PhSCH2)Me2SiC(H):C(Ar)SiMe2(CH2SPh) by Catalytic Activation of the Si-Si Bond:
H.N. Peindy, F. Guyon, I. Jourdain, M. Knorr, D. Schildbach, C. Strohmann,
Organometallics 2006, 25, 1472-1479.

95. Chemistry and Electrochemistry of the Heterodinuclear Complex ClPd(dppm)2PtCl Bond Providing Site Selectivity:
D. Evrard, S. Clement, D. Lucas, B. Hanquet, M. Knorr, C. Strohmann, A. Decken, Y. Mugnier, P.D. Harvey,
Inorg. Chem. 2006, 45, 1305-1315.

94. Understanding Substituent Effects on 29Si Chemical Shifts an Bonding in Disilynes. A Quantum Chemical Analysis:
D. Auer, M. Kaupp, C. Strohmann,
Organometallics 2005, 24, 6331-6337.

93. Selective Si–C Bond Cleavage as Synthetic Entry to a Functionalized Lithiosilane:
C. Strohmann, D. Schildbach, D. Auer,
J. Am. Chem. Soc. 2005, 127, 7968-7969.

92. Complexation of 1,4-Bis(phenylthio)butane on Mercury(II) Salts: Formation of Extended 2D Coordination Polymers:
H.N. Peindy, F. Guyon, M. Knorr, C. Strohmann,
Z. Anorg. Allg. Chem. 2005, 631, 2397-2400.

91. Formation of Extended 1D Coordination Polymers in Tetrathioether Complexes of Mercury(II): Effect of the Organic Substituents on the Crystal Structures of {Si(CH2SR)4}HgBr2 (R = Me, Ph):
H.N. Peindy, F. Guyon, M. Knorr, A.B. Smith, J.A. Farouq, S.A. Islas, D. Rabinovich, J.A. Golen, C. Strohmann,
Inorg. Chem. Commun. 2005, 8, 479-482.

90. Reactivity of Silyl-substituted Heterobimetallic Iron-Platinum Hydride Complexes towards Unsaturated Molecules: Part II. Insertion of Trifluoropropyne and Hexafluorobutyne into the Platinum-Hydride Bond:
M. Knorr, I. Jourdain, F. Villafañe, C. Strohmann,
J. Organomet. Chem. 2005, 690, 1456-1466.

89. Ein hoch diastereomerenangereichertes Lithiumalkyl, konfigurationsstabil bei Raum-temperatur: Darstellung, Molekülstruktur und der diastereodivergente stereo-chemische Reaktionsverlauf in Abhängigkeit des Solvens:
C. Strohmann, B.C. Abele, K. Lehmen, D. Schildbach,
Angew. Chem. 2005, 117, 3196-3199.

88. An Enantiomerically Enriched Silyllithium Compound: The Stereochemical Course of its Transformations:
J. Hörnig, D. Auer, M. Bindl, V.C. Fraaß, C. Strohmann
in Organosilicon Chemistry VI (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2005, S. 502-507.

87. Diastereomerically Enriched α-Lithiated Benzylsilanes:
D. Schildbach, M. Bindl, J. Hörnig, C. Strohmann
in Organosilicon Chemistry VI (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2005, S. 495-501.

86. Synthesis and Reactivity of an Enantiomerically Pure N-Methyl-2-silyl Substituted Pyrrolidine,
K. Strohfeldt, T. Seibel, P. Wich, C. Strohmann
in Organosilicon Chemistry VI (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2005, S. 488-494.

85. Polylithium organic compounds: syntheses and selected molecular structures,
C. Strohmann, D. Schildbach
in The Chemistry of Organolithium Compounds (Editors: Zvi Rappoport and Ilan Marek), John Wiley Sons Limited, Chichester 2004, S.941-996.

84. α-(Lithiomethyl)silanes: About synthetic methods and their special features:
C. Strohmann, D. Schildbach
in Silicon Compounds: Silanes & Silicones, Gelest Katalog 3000-A, Gelest Inc., Morrisville, PA (USA), 2004, S. 83-93.

83. Bis-, Tris- and Tetrakis(lithiomethyl)germanes: New Building Blocks for Organogermanium Compounds:
C. Strohmann, E. Wack,
Z. Naturforsch. 2004, 59b, 1570-1578.

82. Crystal Structures of (+)-Sparteine Surrogate Adducts of Methyllithium and Phenyllithium:
C. Strohmann, K. Strohfeldt, D. Schildbach, M.J. McGrath, P. O’Brien,
Organometallics 2004, 23, 5389-5391.

81. Synthesis and Molecular Structures of Platinum and Mercury Complexes Chelated by (Phenylthiomethyl)silane Ligands:
M. Knorr, H.N. Peindy, F. Guyon, H. Sachdev, C. Strohmann,
Z. Anorg. Allg. Chem. 2004, 630, 1955-1961.

80. “Unexpected” 29Si NMR Chemical Shifts in Heteroatom-Substituted Silyllithium Compounds: A Quantum Chemical Analysis:
D. Auer, M. Kaupp, C. Strohmann,
Organometallics 2004, 23, 3647-3655.

79. The Crystal Structures of a Chiral Aminoalkoxide Cluster and its Adduct with Benzyllithium:
C. Strohmann, T. Seibel, D. Schildbach,
J. Am. Chem. Soc. 2004, 126, 9876-9877.

78. [(Piperidinomethyl)silylmethyl] Cyclopalladated Complexes: Their Synthesis, Reactivity, and Solid State Structures:
D. Schildbach, M. Arroyo, K. Lehmen, S. Martín-Barrios, F. Villafañe, C. Strohmann,
Organometallics 2004, 23, 3228-3238.

77. 3-Silaoxetane and 3-silathietane: structure and reactivity studies on the basis of spectroscopic data and theoretical calculations:
I. Pavel, K. Strohfeldt, C. Strohmann, W. Kiefer,
Inorg. Chim. Acta 2004, 357, 1920-1930.

76. Enantiodivergenz bei Umsetzungen einer hoch enantiomerenangereicherten Silyllithium-Verbindung mit Benzylhalogeniden: Steuerung von Inversion und Retention durch Wahl des Halogenids:
C. Strohmann, M. Bindl, V.C. Fraaß, J. Hörnig,
Angew. Chem. 2004, 116, 1029-1032.

75. The Crystal Structures of the Chiral Alkyllithium Bases [n-BuLi∙(–)-Sparteine]2 and [Et2O∙(i-PrLi)2∙(–)-Sparteine]:
C. Strohmann, K. Strohfeldt, D. Schildbach,
J. Am. Chem. Soc. 2003, 125, 13672-13673.

74. Molekülstruktur von tBuLi∙(–)-Spartein im Festkörper: Die erste monomere BuLi-Verbindung:
C. Strohmann, T. Seibel, K. Strohfeldt,
Angew. Chem. 2003, 115, 4669-4671.

73. Understanding Substituent Effects on 29Si Chemical Shifts and Bonding in Disilenes. A Quantum Chemical Analysis:
D. Auer, C. Strohmann, A. Arbuznikov, M. Kaupp,
Organometallics 2003, 22, 2442-2449.

72. Synthesis and Reactivity of Dinuclear Iron-Platinum, Chromium-Platinum, Molybdenum-Platinum and Tungsten-Platinum Complexes with Bridging Carbonyl, Isocyanide and Aminocarbyne Ligands. An Empirical Study on the Parameters decisive for the Bonding Mode of the Isocyanide Ligand:
M. Knorr, I. Jourdain, D. Lentz, S. Willemsen, C. Strohmann,
Organomet. Chem. 2003, 684, 216-229.

71. Syntheses and Crystal Structures of Highly Diastereomerically Enriched Lithiated Benzylsilanes in the Presence of External Donor Molecules: Experiment and Theory:
C. Strohmann, D.H.M. Buchold, T. Seibel, K. Wild, D. Schildbach,
Eur. J. Inorg. Chem. 2003, 3453-3463.

70. (Phenylthiomethyl)silanes and (Butyltelluromethyl)silanes as Novel Bifunctional Ligands for the Construction of Dithioether-, Ditelluroether- and transition Metal-Silicon Complexes:
M. Knorr, F. Guyon, I. Jourdain, S. Kneifel, J. Frenzel, C. Strohmann,
Inorg. Chim. Acta 2003, 350, 455-466.

69. Selective Transformations Starting from Diastereomerically Enriched Lithiated Benzylsilane:
C. Strohmann, D.H.M. Buchold, K. Wild, D. Schildbach
in Organosilicon Chemistry V (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2003, S. 155-166.

68. Syntheses of Silyllithium Reagents Starting from Tetraorganosilanes,
J. Hörnig, D. Auer, C. Strohmann
in Organosilicon Chemistry V (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2003, S. 150-154.

67. 29Si NMR Chemical Shifts of four- and five-Membered Organosilacycles: Experimental and Theoretical Studies:
K. Strohfeldt, K. Andres, R. Bertermann, E. Wack, M. Kaupp, C. Strohmann
in Organosilicon Chemistry V (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2003, S. 329-333.

66. Synthesis of a Highly Enantiomerically Enriched Silyllithium Compound,
D. Auer, J. Hörnig, C. Strohmann in Organosilicon Chemistry V (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2003, S. 167-170.

65. Trigonal Prismatic Structure of Tris(Butadiene)-Molybdenum and Related Complexes Revisited: Diolefin or Metallacyclopentene Coordination?:
M. Kaupp, T. Kopf, A. Murso, D. Stalke, C. Strohmann, J.R. Hanks, F.G.N. Cloke, P.B. Hitchcock,
Organometallics 2002, 21, 5021-5028.

64. Bis{[diphenyl(piperidinomethyl)silyl]methyl}cadmium and -magnesium:
C. Strohmann, D. Schildbach,
Acta Cryst. C 2002, 58, m447-m449.

63. Enantiomerically Enriched “Carbanions”: Studies on the Stereochemical Course of Selective Transformations of Metal Alkyls:
C. Strohmann, B.C. Abele, K. Lehmen, F. Villafañe, L. Sierra, S. Martín-Barrios, D. Schildbach,
J. Organomet. Chem. 2002, 661, 149-158.

62. A highly diastereomerically enriched benzyllithium compound – the molecular structure and the stereochemical course of its transformations:
C. Strohmann, K. Lehmen, K. Wild, D. Schildbach,
Organometallics 2002, 21, 3079-3081.

61. Synthesis of a highly enantiomerically enriched silyllithium compound:
C. Strohmann, J. Hörnig and D. Auer,
J. Chem. Soc., Chem. Commun. 2002, 766-767.

60. Synthesis, Reactivity and Molecular Structures of Bis(diphenylphosphanyl)methane-bridged Heterobimetallic Iron-Platinum Isocyanide Complexes: Breaking and Formation of Metal-Metal Bonds:
M. Knorr, I. Jourdain, G. Crini, K. Frank, H. Sachdev, C. Strohmann,
Eur. J. Inorg. Chem. 2002, 2419-2426.

59. Vibrational Studies and Density Functional Theory Calculations On 3-Silaoxetanes and 3-Silathietanes, 
I. Pavel, D. Moigno, W. Kiefer, K. Strohfeldt, C. Strohmann
in Eighteenth International Conference on Raman Spectroscopy, John Wiley & Sons, New York, 2002, S. 601.

58. A Monolithiated and its Related 1,3-Dilithiated Benzylsilane: Syntheses and Crystal Structures:
C. Strohmann, K. Lehmen, A. Ludwig, D. Schildbach,
Organometallics 2001, 20, 4138-4140.

57. Heterobimetallic intermediates in alkene insertion reactions into a Pd-acetyl bond:
P. Braunstein, J. Durand, M. Knorr, C. Strohmann,
J. Chem. Soc., Chem. Commun. 2001, 211-212.

56. Crystal Structures and 29Si NMR Calculations of Amino-functionalized Silyllithium Compounds:
C. Strohmann, O. Ulbrich, D. Auer,
Eur. J. Inorg. Chem. 2001, 1013-1018.

55. Oxidative Addition of Iodine, Idomethane and Iodobenzene to the Rhodium Phosphino Enolate Complex [Rh{Ph2PCH···C(···O)Ph}(CO)(PPh3)] and Carbon Monoxide Insertion into the Resulting Rh-Carbon Bond of [Rh{Ph2PCH···C(···O)Ph}(Me) (I)(CO)(PPh3)]:
P. Braunstein, Y. Chauvin, J. Fischer, H. Olivier, C. Strohmann, D.V. Toronto,
New J. Chem. 2000, 24, 437-445.

54. Verbrückende Koordination von Gallium-Gallium-Bindungen durch Chelatliganden - Grenzen der Beständigkeit von Digallium-Verbindungen:
W. Uhl, L. Cuypers, K. Schüler, T. Spies, C. Strohmann, K. Lehmen,
Z. Anorg. Allg. Chem. 2000, 626, 1526-1534.

53. Synthesis and molecular structure of the unsymmetrically substituted magnesium alkyl Mg(Bun){CH[SPh][SiPh2(CH2NC4H10)]}:
C. Strohmann, B.C. Abele, D. Schildbach, K. Strohfeldt,
J. Chem. Soc., Chem. Commun. 2000, 865-866.

52. Tris- and Tetrakis(lithiomethyl)silanes: An Easy Access to New Building Blocks for Organosilicon Compounds:
C. Strohmann, S. Lüdtke, O. Ulbrich,
Organometallics 2000, 19, 4223-4227.

51. Reactivity of Silyl-substituted Heterobimetallic Iron-Platinum Hydride Complexes towards Unsaturated Molecules. Part I. Alkyne Insertions into the Platinum-Hydride Bond, Phosphine-induced σ-Alkenyl-µ-Vinylidene Rearrangements and Formation of µ-Isonitrile Complexes:
M. Knorr, C. Strohmann,
Eur. J. Inorg. Chem. 2000, 241-252.

50. Ladder Structure of a Lithium Organyl: Synthesis and Crystal Structure of a Mixed Aggregate of n-BuLi and an (Aminomethyl)(lithiomethyl)silane:
C. Strohmann, B.C. Abele,
Organometallics 2000, 19, 4173-4175.

49. Synthesis and Reactivity of Novel 1,2-Disilacyclopentanes,
C. Strohmann, O. Ulbrich
in Organosilicon Chemistry IV (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 2000, S.220-225.

48. Trends in Organic Chemistry in 1998 Part 1:
N. Goldberg, H.-U. Siehl, T. Müller, C. Strohmann, B. Breit, B.König, K. Johnsson, U. Diederichsen,
Nachr. Chem. Tech. Lab. 1999, 47, 153-175.

47. Jahresrückblick "polare Metallalkyle":
C.Strohmann,
Nachr. Chem. Tech. Lab. 1999, 47, 153.

46. Migratory insertion reactions of norbornene, norbornadiene and 7-oxanorbornene derivatives into the palladium-carbon bond of heterodinuclear Fe-Pd-Acyl complexes. Substrate influence on the Pd coordination sphere and crystal structure of [cyclic] [(OC)3Fe{µ-Si(OMe)2(OMe)}(m-dppa)Pd{C9H9NO3C(:O)Me}]:
P. Braunstein, J. Cossy, M. Knorr, C. Strohmann, P. Vogel,
New J. Chem. 1999, 23, 1215-1222.

45. Syntheses, Structures, and Reactivity of Dinuclear Molybdenum-Platinum and Tungsten-Platinum Complexes with Bridging Carbonyl, Sulfur Dioxide, Isonitrile, and Aminocarbyne Ligands and a dppa Backbone (dppa = Ph2PNHPPh2):
M. Knorr, C. Strohmann,
Organometallics 1999, 18, 248-257.

44. (Phenylthiomethyl)silanes as New Bifunctional Assembling Ligands for the Construction of Heterometallic Complexes:
M. Knorr, S. Kneifel, C. Strohmann
in Organosilicon Chemistry III (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 1998, S.211-216.

43. Synthesis of 1,3-Disilacyclobutanes, 1,3-Digermacyclobutanes, and 1-Germa-3- silacyclobutanes with new 1,3-Dimetalated Organoelement Building Blocks,
C. Strohmann, E. Wack
in Organosilicon Chemistry III (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 1998, S.217-222.

42. New Organosilicon Reagents: Synthesis, Structure and Reactivity of (Lithiomethyl)(aminomethyl)silanes:
B.C. Abele, C. Strohmann
in Organosilicon Chemistry III (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 1998, S.206-210.

41. Unexpected Reactivity of 1,2-Bis(bromodiphenylmethyl)-1,1,2,2-tetramethyldisilane:
F. Pillong, O. Schütt, C. Strohmann
in Organosilicon Chemistry III (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 1998, S. 281-285.

40. Synthesis, Reactivity and Molecular Structures of Bis(diphenylphosphinyl)amine- and Bis(diphenylphosphinyl)amide-bridged Heterobimetallic m-Isonitrile- and m-Aminocarbyne Complexes (Fe-Pt):
M. Knorr, C. Strohmann,
Eur. J. Inorg. Chem. 1998, 495-499.

39. Konformationskontrolle in Polymetall-Mesocyclen durch eine Metall-Metall-Bindung: das erste Beispiel für eine Hg-Cu-Wechselwirkung:
M. Benard, U. Bodensieck, P. Braunstein, M. Knorr, M. Strampfer, C. Strohmann,
Angew. Chem. 1997, 109, 2890-2893.

38. First aminosilyl bridging ligand in a bimetallic complex: Structure of [(OC)3{(Me2N)2(MeO)P}Fe(µ-Si(OMe)2(NMe2)}Cu(PPh3)]:
P. Braunstein, C. Stern, C. Strohmann, N. Tong,
J. Chem. Soc., Chem. Commun. 1996, 2237-2238.

37. Lehrbuch der Anorganischen Chemie, von Holleman/Wiberg, 101., verbesserte und stark erweiterte Auflage, deGruyter, 1995:
C. Strohmann,
Nachr. Chem. Tech. Lab. 1996, 44, 806.

36. Reduktive Kohlenstoff-Schwefel-Bindungsspaltung: Ein einfacher Zugang zu nicht stabilisierten (Lithiomethyl)aminen:
C. Strohmann, B.C. Abele,
Angew. Chem. 1996, 108, 2514-2516.

35. Reactivity of Silylated Dinuclear Iron-Platinum Acyl Complexes: Formation of µ-Vinylidene Complexes and Crystal Structures of the Acyl Complex [(OC)3{(MeO)3Si}Fe(µ-dppm)Pt{C(O)Me}(t-BuNC)] and the µ-Vinylidene Complex [(OC)3Fe{-C=C(H)Ph}(m-dppm)Pt(PPh3)]:
M. Knorr, C. Strohmann, P. Braunstein,
Organometallics 1996, 15, 5653-5663.

34. Bis(lithiomethyl)sulfid: Ein unerwartet stabiler 1,3-dilithiierter Synthesebaustein:
C. Strohmann,
Angew. Chem. 1996, 108, 600-601.

33. New Bis(lithiomethyl)silanes. Building Blocks for Organosilanes:
C. Strohmann, S. Lüdtke, E. Wack,
Chem. Ber. 1996, 129, 799-805.

32. Mono-, Bis-, Tris- and Tetrakis(lithiomethyl)silanes: New Building Blocks for Organosilicon Compounds:
C. Strohmann, S. Lüdtke
in Organosilicon Chemistry II (Hrsg.: N. Auner, J. Weis), VCH, Weinheim, 1996, S.499-504.

29. Binding and functional properties of hexocyclium and sila-hexocyclium derivatives to muscarinic receptor subtypes:
M. Waelbroeck, J. Camus, M. Tastenoy, R. Feifel, E. Mutschler, R. Tacke, C. Strohmann, K. Rafeiner, J.F. Rodrigues de Miranda, G. Lambrecht,
Br. J. Pharmacol. 1994, 112, 505-514.

28. New organosilicon polymers for ceramics applications:
D. Seyferth, C. Strohmann, N.R. Dando, A.J. Perrotta, J.P. Gardner, Mater. Res. Soc. Symp. Proc. 1994, 327, 191-199.

27. Methylhydridopolysilazane and its pyrolytic conversion to silicon nitride-silicon carbide (Si3N4/SiC) ceramics:
N.R. Dando, A.J. Perrotta, C. Strohmann, R.M. Stewart, D. Seyferth,
Chem. Mater. 1993, 5, 1624-1630.

26. Neue zwitterionische λ5-Spirosilicate: Synthese, Einkristall-Röntgenstrukturanalysen und Festkörper-NMR-Untersuchungen:
R. Tacke, A. Lopez-Mras, J. Sperlich, C. Strohmann, W.F. Kuhs, G. Mattern, A. Sebald,
Chem. Ber. 1993, 126, 851-861.

25. Methylhydridopolysilazane and its pyrolytic conversion to Si3N4/SiC ceramics:
N.R. Dando, A.J. Perrotta, C. Strohmann, R.M. Stewart,
Report 1993, 93 Abstr. No. 350, 494.

24. Synthesis and useful reactions of organosilicon polymeric precursors for ceramics:
D. Seyferth, C. Strohmann, H.J. Tracy, J.L. Robison,
Report 1992, 92, Abstr. No. 241, 210.

23. Synthesis and useful reactions of organosilicon polymeric precursors for ceramics:
D. Seyferth, C. Strohmann, H.J. Tracy, J.L. Robison,
Mater. Res. Soc. Symp. Proc. 1992, 249, 3-14.

22. Bis[3,4,5,6-tetrabromo-1,2-benzenediolato(2-)}(pyrrolidiniomethyl)silicate- acetonitrile-solvate, [(C6Br4O2)2SiCH2(H)NC4H8CH3CN]: Synthesis and crystal and molecular structure of a zwitterionic λ5-spirosilicate:
R. Tacke, J. Sperlich, C. Strohmann, B. Frank, G. Mattern,
Z. Kristallogr. 1992, 199, 91-98.

21. Stereoselective interaction of procyclidine, hexahydrodifenidol, hexbutinol and oxyphencyclimine, and of related antagonists, with four muscarinic receptors:
M. Waelbroeck, J. Camus, M. Tastenoy, E. Mutschler, C. Strohmann, R. Tacke, L. Schjelderup, A. Aasen, G. Lambrecht, J. Christophe,
Eur. J. Pharmacol. 1992, 227, 33-42.

20. Preparation of quaternized 1,1-dicycloalkyl-4-amino-2-butyn-1-ols as selective antimuscarinics,
G. Lambrecht, E. Mutschler, R. Tacke, L.K. Choo, C. Strohmann,
Ger. Offen. 1991.

19. Cyclohexyl(4-fluorophenyl)(3-piperidinopropyl)silanol [p-fluoro-hexahydrosila-dife-nidol (p-F-HHSiD)] and derivatives: synthesis and antimuscarinic properties:
R. Tacke, K. Mahner, C. Strohmann, B. Forth, E. Mutschler, T. Friebe, G. Lambrecht,
J. Organomet. Chem. 1991, 417, 339-353.

18. Bis[2,3-naphthalenediolato(2-)](pyrrolidiniomethyl)silicat-Acetonitril-Solvat: Synthese sowie Kristall und Molekülstruktur eines zwitterionischen λ5-Spirosilicats:
R. Tacke, J. Sperlich, C. Strohmann, G. Mattern,
Chem. Ber. 1991, 124, 1491-1496.

17. Bioorganosilicon chemistry - recent results:
R. Tacke, S. Brakmann, M. Kropfgans, C. Strohmann, F. Wuttke, G. Lambrecht, E. Mutschler, P. Proksch, H.-M. Schiebel, L. Witte
in Frontiers of Organosilicon Chemistry (A.R. Bassindale and P.P.Gaspar, Hrsg.), Bookcraft (Bath) Ltd., Cambridge (England) 1991, S.218-228.

16. Enantiomers of the Muscarinic Antagonist 1-Cyclohexyl-1-(4-fluorophenyl)-4-piperidino-1-butanol (p-Fluorohexahydrodifenidol): Synthesis, Absolute Configuration, and Enantiomeric Purity:
C. Strohmann, S. Bauerecker, H.-K. Cammenga, P.G. Jones, E. Mutschler, G. Lambrecht, R. Tacke,
Liebigs Ann. Chem. 1991, 523-527.

15. Stereoselectivity of (R)- and (S)-hexahydro-difenidol binding to neuroblastoma M1, cardiac M2, pancreatic M3, and striatum M4 muscarinic receptors:
M. Waelbroeck, J. Camus, M. Tastenoy, E. Mutschler, C. Strohmann, R. Tacke, G. Lambrecht, J. Chistophe,
Chirality 1991, 3, 118-123.

14. Binding affinities of hexahydro-difenidol and hexahydro-sila-difenidol analogs at four muscarinic receptor subtypes: constitutional and stereochemical aspects:
M. Waelbroeck, J. Camus, M. Tastenoy, E. Mutschler, C. Strohmann, R. Tacke, G. Lambrecht, J. Chistophe,
Eur. J. Pharmacol. 1991, 206, 95-103.

13. Bis(2,3-naphthalindiolato)[2-(pyrrolidinio)ethyl]silicat: Synthese und strukturelle Charakterisierung eines zwitterionischen λ5-Spirosilicats:
C. Strohmann, G. Mattern, W.F. Kuhs, R. Tacke,
J. Organomet. Chem. 1991, 403, 63-71.

12. Selective labeling of muscarinic M1 receptors in calf superior cervical ganglia by [3H](±)-telenzepine:
R. Feifel, J.F. Rodrigues de Miranda, C. Strohmann, R. Tacke, A.J. Aasen, E. Mutschler, G. Lambrecht,
Eur. J. Pharmacol. 1991, 195, 115-123.

 

11. Pharmacokinetic properties of the antimuscarinic drug [3H]-hexahydro-sila-difenidol in the rat:
N.M. Rettenmayr, J.F. Rodrigues de Miranda, N.V.M. Rijntjes, F.G.M. Russel, C.A.M. van Ginneken, C. Strohmann, R. Tacke, G. Lambrecht, E. Mutschler,
Naunyn-Schmiedeberg´s Arch. Pharmacol. 1990, 342, 146-152

10. Stereoselective inhibition of muscarinic receptor subtypes by the enantiomers of hexahydro-difenidol and acetylenic analogues:
R. Feifel, M. Wagner-Röder, C. Strohmann, R. Tacke, M. Waelbroeck, J. Christophe, E. Mutschler, G. Lambrecht,
Br. J. Pharmacol. 1990, 99, 455.

9. Stereoselectivity of the interaction of muscarinic antagonists with their receptors:
M. Waelbroeck, M. Tastenoy, J. Camus, R. Feifel, E. Mutschler, C. Strohmann, R. Tacke, G. Lambrecht, J. Christophe,
Trends Pharmacol. Sci. 1989, 10, Suppl. 65-69.

8. Pharmacology of hexahydrodifenidol, hexahydrosiladifenidol and related selective muscarinic antagonists:
G. Lambrecht, R. Feifel, U. Moser, M. Wagner-Röder, L.K. Choo, J. Camus, M. Tastenoy, M. Waelbroeck, C. Strohmann, R. Tacke, J.F. Rodrigues de Miranda, J. Christophe, E. Mutschler,
Trends Pharmacol. Sci. 1989, 10, Suppl. 60-64.

7. Affinity profiles of hexahydro-sila-difenidol analogs at muscarinic receptor subtypes:
G. Lambrecht, R. Feifel, M. Wagner-Röder, C. Strohmann, H. Zilch, R. Tacke, M. Waelbroeck, J. Christophe, H. Boddeke, E. Mutschler,
Eur. J. Pharmacol. 1989, 168, 71-80.

6. Binding and functional properties of antimuscarinics of the hexocyclium/sila- hexocyclium and hexahydro-diphenidol/hexahydro-sila-difenidol type to muscarinic receptor subtypes:
M. Waelbroeck, M. Tastenoy, J. Camus, J. Christophe, C. Strohmann, H. Linoh, H. Zilch, R.Tacke, E. Mutschler, G. Lambrecht,
Br. J. Pharmacol. 1989, 98, 197-205.

5. Darstellung und Eigenschaften der Enantiomere des selektiven Antimuscarinikums 1-Cyclohexyl-1-phenyl-4-piperidino-1-butanol (Hexahydro-Difenidol):
R. Tacke, C. Strohmann, S. Sarge, H.K. Cammenga, D. Schomburg, E. Mutschler, G. Lambrecht,
Liebigs Ann. Chem. 1989, 137-143.

4. Synthesis of the selective antimuscarinic agent 4-{[cyclohexylhydroxy(2-methoxy-phenyl)silyl]methyl}-1,1-dimethylpiperazinium methyl sulfate (o-methoxysila- hexocyclium methyl sulfate):
R. Tacke, K. Rafeiner, C. Strohmann, E. Mutschler, G. Lambrecht,
Appl. Organomet. Chem. 1989, 3, 129-132.

3. Presynaptic muscarinic receptors mediating inhibition of neurogenic contractions in rabbit vas deferens are of the ganglionic M1-type:
M. Eltze, G. Gmelin, J. Wess, C. Strohmann, R. Tacke, E. Mutschler, G. Lambrecht,
Eur. J. Pharmacol. 1988, 158, 233-242.

2. p-Fluorohexahydro-siladifenidol: The first M2β-selective muscarinic antagonist:
G. Lambrecht, R. Feifel, B. Forth, C. Strohmann, R. Tacke, E. Mutschler,
Eur. J. Pharmacol. 1988, 152, 193-194.

1. σ-Methoxy-sila-hexocyclium: a new quaternary M1-selective muscarinic antagonist:   
G. Lambrecht, G. Gmelin, K. Rafeiner, C. Strohmann, R. Tacke, E. Mutschler,
Eur. J. Pharmacol. 1988, 151, 155-156.

Statistik der Artikel

Medium Anzahl Impact-Faktor
J. Am. Chem. Soc. 16 14.695
Angew. Chem. 34 12.257
Chem. Commun. 15 6.164
Chem. Eur. J.  14 5.160
Inorg. Chem.  17 4.850
Organometallics  20 3.862
Dalton Trans. 8 4.052
Eur. J. Inorg. Chem. 22 2.578

Location & approach

The campus of TU Dort­mund University is located close to interstate junction Dort­mund West, where the Sauerlandlinie A 45 (Frankfurt-Dort­mund) crosses the Ruhrschnellweg B 1 / A 40. The best interstate exit to take from A 45 is "Dort­mund-Eichlinghofen" (closer to Campus Süd), and from B 1 / A 40 "Dort­mund-Dorstfeld" (closer to Campus Nord). Signs for the uni­ver­si­ty are located at both exits. Also, there is a new exit before you pass over the B 1-bridge leading into Dort­mund.

To get from Campus Nord to Campus Süd by car, there is the connection via Vogelpothsweg/Baroper Straße. We recommend you leave your car on one of the parking lots at Campus Nord and use the H-Bahn (suspended monorail system), which conveniently connects the two campuses.

TU Dort­mund University has its own train station ("Dort­mund Uni­ver­si­tät"). From there, suburban trains (S-Bahn) leave for Dort­mund main station ("Dort­mund Hauptbahnhof") and Düsseldorf main station via the "Düsseldorf Airport Train Station" (take S-Bahn number 1, which leaves every 20 or 30 minutes). The uni­ver­si­ty is easily reached from Bochum, Essen, Mülheim an der Ruhr and Duisburg.

You can also take the bus or subway train from Dort­mund city to the uni­ver­si­ty: From Dort­mund main station, you can take any train bound for the Station "Stadtgarten", usually lines U41, U45, U 47 and U49. At "Stadtgarten" you switch trains and get on line U42 towards "Hombruch". Look out for the Station "An der Palmweide". From the bus stop just across the road, busses bound for TU Dort­mund University leave every ten minutes (445, 447 and 462). Another option is to take the subway routes U41, U45, U47 and U49 from Dort­mund main station to the stop "Dort­mund Kampstraße". From there, take U43 or U44 to the stop "Dort­mund Wittener Straße". Switch to bus line 447 and get off at "Dort­mund Uni­ver­si­tät S".

The H-Bahn is one of the hallmarks of TU Dort­mund University. There are two stations on Campus Nord. One ("Dort­mund Uni­ver­si­tät S") is directly located at the suburban train stop, which connects the uni­ver­si­ty directly with the city of Dort­mund and the rest of the Ruhr Area. Also from this station, there are connections to the "Technologiepark" and (via Campus Süd) Eichlinghofen. The other station is located at the dining hall at Campus Nord and offers a direct connection to Campus Süd every five minutes.

The AirportExpress is a fast and convenient means of transport from Dortmund Airport (DTM) to Dortmund Central Station, taking you there in little more than 20 minutes. From Dortmund Central Station, you can continue to the university campus by interurban railway (S-Bahn). A larger range of international flight connections is offered at Düsseldorf Airport (DUS), which is about 60 kilometres away and can be directly reached by S-Bahn from the university station.

The facilities of TU Dortmund University are spread over two campuses, the larger Campus North and the smaller Campus South. Additionally, some areas of the university are located in the adjacent "Technologiepark".

Site Map of TU Dortmund University (Second Page in English).