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Publications

Hülya Sak, Matthias Mawick, Norbert Krause
Sustainable Gold Catalysis in Water Using Cyclodextrin-tagged NHC-Gold Complexes
ChemCatChem 201911. 5821-5829  (Special Issue on Sustainable and Affordable Chemistry to Meet Future Challenges in the Pharmaceutical Industry) dx.doi.org/10.1002/cctc.201901658

Anja Wiegand, Vera Wiese, Britta Glowacki, Ljuba Iovkova, Ralf Schirrmacher, Klaus Jurkschat, Norbert Krause
GlucoSiFA and LactoSiFA: New Types of Carbohydrate-Tagged Silicon-Based Fluoride Acceptors for 18F-Positron Emission Tomography (PET)
Synthesis 2019, 51, 1196-1206  (Golden Anniverary Issue - Part II) dx.doi.org/10.1055/s-0037-1611656

Mark C. Bagley, Klaus Banert, Norbert Krause, Miguel Yus (Eds.)
Science of Synthesis Knowledge Updates 2019/1
Thieme, Stuttgart, 2019.

Mogens Brøndsted Nielsen, Norbert Krause, Jörg Rademann, Christopher A. Ramsden, Hans-Ulrich Reissig (Eds.)
Science of Synthesis Knowledge Updates 2018/1
Thieme, Stuttgart, 2018.

Mateja Klika Škopić, Suzanne Willems, Bernd Wagner, Justin Schieven, Norbert Krause, Andreas Brunschweiger
Exploration of a Au(I)-mediated Three-component reaction for the Synthesis of DNA-tagged Highly Substituted Spirocycles
Org. Biomol. Chem. 2017, 15, 8648-8654. dx.doi.org/10.1039/C7OB02347B

New Surfactants for Chemistry in Water
Curr. Opin. Green Sust. Chem. 20177, 18-22. doi.org/10.1016/j.cogsc.2017.06.009

John A. Joule, Norbert Krause, Martin Oestreich, Jörg Rademann, Ernst Schaumann, Thomas Wirth (Eds.)
Science of Synthesis Knowledge Updates 2017/1
Thieme, Stuttgart, 2017.

Linda Lempke, Hülya Sak, Michael Kubicki, Norbert Krause
Gold-catalyzed Cycloisomerization of Trifluoromethylated Allenols: Sustainability and Mechanistic Studies
Org. Chem. Front. 2016, 3, 1514-1519. dx.doi.org/10.1039/C6QO00423G

Bernd Wagner, Katrin Belger, Stefan Minkler, Volker Belting, Norbert Krause
Sustainable Gold Catalysis: Synthesis of New Spiroacetals 
Pure Appl. Chem. 201688, 391-399. dx.doi.org/10.1515/pac-2016-0406

Linda Lempke, Andrea Ernst, Fabian Kahl, Ralf Weberskirch, Norbert Krause
Sustainable Micellar Gold Catalysis - Poly(2-oxazolines) as Versatile Amphiphiles 
Adv. Synth. Catal. 2016358, 1491-1499. dx.doi.org/10.1002/adsc.201600139

Bernd Wagner, Wolf Hiller, Hiroaki Ohno, Norbert Krause
Gold-catalyzed Three-component Spirocyclization: A One-pot Approach to Functionalized Pyrazolidines
Org. Biomol. Chem. 201614, 1579-1583. dx.doi.org/10.1039/C5OB02453F

Katrin Belger, Norbert Krause
Smaller, Faster, Better: Modular Synthesis of Unsymmetrical Ammonium Salt-tagged NHC-Gold(I) Complexes and Their Application as Recyclable Catalysts in Water
Org. Biomol. Chem. 201513, 8556-8560. dx.doi.org/10.1039/C5OB01286D

Linda Lempke, Tobias Fischer, Jérémy Bell, Werner Kraus, Knut Rurack, Norbert Krause
Gold-catalyzed Allene Cycloisomerization for Pyrrole Synthesis: Towards Highly Fluorinated BODIPY Dyes
Org. Biomol. Chem. 201513, 3787-3791. dx.doi.org/10.1039/C4OB02671C 

Viola Breker, Hülya Sak, Giusy Baracchi-Krause, Norbert Krause
Synthesis and Properties of a Biotin-tagged NHC-Gold Complex
Tetrahedron Lett. 201556, 3390-3392. dx.doi.org/10.1016/j.tetlet.2015.01.023

Katrin Belger, Norbert Krause
Ammonium Salt-tagged IMesAuCl Complexes and their Application in Gold-catalyzed Cycloisomerization Reactions in Water
Eur. J. Org. Chem. 2015, 220-225. dx.doi.org/10.1002/ejoc.201403153

Alexandre Alexakis, Norbert Krause, Simon Woodward (Eds.)
Copper-Catalyzed Asymmetric Synthesis, Wiley-VCH, Weinheim, 2014.

Alexandre Alexakis, Norbert Krause, Simon Woodward (Eds.)
Copper-Catalyzed Asymmetric Conjugate Addition
in: “Copper-Catalyzed Asymmetric Synthesis”, Wiley-VCH, Weinheim, 2014, pp. 33-68.

Mogens Brøndsted Nielsen, Norbert Krause, Ilan Marek, Ernst Schaumann, Thomas Wirth (Eds.)
Science of Synthesis Knowledge Updates 2014/2
Thieme, Stuttgart, 2014.

Erick M. Carreira, Norbert Krause, Martin Oestreich, Bernd J. Plietker, Patrick G. Steel (Eds.)
Science of Synthesis Knowledge Updates 2014/1
Thieme, Stuttgart, 2014.

Stefan R. K. Minkler, Nicholas A. Isley, Daniel J. Lippincott, Norbert Krause, Bruce H. Lipshutz
Leveraging the Micellar Effect: Gold-Catalyzed Dehydrative Cyclizations in Water at Room Temperature
Org. Lett. 201416, 724-726. dx.doi.org/10.1021/ol403402h

Norbert Krause
Organogold Chemistry
in: “Organometallics in Synthesis – Fourth Manual“ (Bruce H. Lipshutz, Ed.), Wiley, New York, 2013, pp 429-540.

Yoshinari Sawama, Kyoshiro Shibata, Yuka Sawama, Masato Takubo, Yasunari Monguchi, Norbert Krause, Hironao Sajiki
Iron-Catalyzed Ring-Opening Azidation and Allylation of Tetrahydrofuran Derivatives
Org. Lett. 201315, 5282-5285. dx.doi.org/10.1021/ol402511r

Jörg Erdsack, Norbert Krause
An Approach Towards Azafuranomycin Analogs by Gold-catalyzed Cycloisomerization of Allenes: Synthesis of (aS,2R)-(2,5-Dihydro-1H-pyrrol)glycine
Beilstein J. Org. Chem. 20139, 1936-1942. dx.doi.org/10.3762/bjoc.9.229

Tao Sun, Carl Deutsch, Norbert Krause
Combined Coinage Metal Catalysis in Natural Product Synthesis: Total Synthesis of (+)-Varitriol and Seven Analogs
Org. Biomol. Chem. 201210, 5965-5970. dx.doi.org/10.1039/C2OB25069A

Christian Winter, Norbert Krause
Gold-Catalyzed Addition Reactions to Allenes
in: „Modern Gold-Catalyzed Synthesis“ (A. S. K. Hashmi, F. D. Toste, Eds.), Wiley-VCH, Weinheim, 2012, pp. 363-389.

Norbert Krause
Golden Times for Allenes
in: „Innovative Catalysis in Organic Synthesis: Oxidation, Hydrogenation, and C-X Bond Forming Reactions“ (P. G. Andersson, Ed.), Wiley-VCH, Weinheim, 2012, pp. 195-209.

Norbert Krause
Die fabelhafte Welt der Allene
Nachr. Chem. 201260, 118-121.

Norbert Krause, Özge Aksin-Artok, Martta Asikainen, Viola Breker, Carl Deutsch, Jörg Erdsack, Hong-Tao Fan, Birgit Gockel, Stefan Minkler, Manojkumar Poonoth, Yoshinari Sawama, Yuka Sawama, Tao Sun, Frank Volz, Christian Winter
Combined Coinage Metal Catalysis for the Synthesis of Bioactive Molecules
J. Organomet Chem. 2012704, 1-8. dx.doi.org/10.1016/j.jorganchem.2012.01.008

Erick M. Carreira, Józef Drabowicz, Alois Fürstner, Norbert Krause, Mark G. Moloney (Eds.)
Science of Synthesis Knowledge Updates 2011/2
Thieme, Stuttgart, 2011.

Norbert Krause
M. Harmata (Ed.): Silver in Organic Chemistry (Book Review)
Nachr. Chem. 201159, 996.

Stefan R. K. Minkler, Bruce H. Lipshutz, Norbert Krause
Gold Catalysis in Micellar Systems
Angew. Chem. 2011123, 7966-7969. dx.doi.org/10.1002/ange.201101396
Angew. Chem. Int. Ed. 201150, 7820-7823. dx.doi.org/10.1002/anie.201101396

Muhammed Üçüncü, Erman Karakus, Melih Kus, Gürkan Eray Akpinar, Özge Aksin-Artok, Norbert Krause, Sila Karaca, Nuran Elmaci, Levent Artok
Rhodium- and Palladium-Catalyzed 1,5-Substitution Reactions of 2-En-4-yne Acetates and Carbonates with Organoboronic Acids
J. Org. Chem.201176, 5959-5971. dx.doi.org/10.1021/jo200201r

Norbert Krause, Christian Winter
Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles
Chem. Rev. 2011111, 1994-2009. dx.doi.org/10.1021/cr1004088

Manojkumar Poonoth, Norbert Krause
Cycloisomerization of Bifunctionalized Allenes: Synthesis of 3(2H)-Furanones in Water
J. Org. Chem. 201176, 1934-1936. dx.doi.org/10.1021/jo102416e

Özge Aksin-Artok, Norbert Krause
Combined Rhodium/Gold Catalysis: From Propargyloxiranes to 2,5-Dihydrofurans in One Pot
Adv. Synth. Catal. 2011353, 385-391. dx.doi.org/10.1002/adsc.201000903

Yoshinari Sawama, Koichi Kawamoto, Hiroyuki Satake, Norbert Krause, Yasuyuki Kita
Regioselective Gold-Catalyzed Allylative Ring Opening of 1,4-Epoxy-1,4-dihydronaphthalenes
Synlett  2010, 2151-2155 dx.doi.org/10.1055/s-0030-1258528

Norbert Krause, Özge Aksin-Artok, Viola Breker, Carl Deutsch, Birgit Gockel, Manojkumar Poonoth, Yoshinari Sawama, Yuka Sawama, Tao Sun and Christian Winter
Combined Coinage Metal Catalysis for the Synthesis of Bioactive Molecules
Pure Appl. Chem. 2010, 82,1529-1536 dx.doi.org/10.1351/PAC-CON-09-09-23

Sébastien Belot, Adrien Quintard, Norbert Krause, Alexandre Alexakis
Organocatalyzed Conjugate Addition of Carbonyl Compounds to Nitrodienes/Nitroenynes and Synthetic Applications
Adv. Synth. Catal. 2010352, 667-695 dx.doi.org/10.1002/adsc.200900814

Birgit Gockel, Norbert Krause
Synthesis of Bicyclic Ethers by a Gold/Palladium/Gold-Catalyzed Cyclization/Cross Coupling Sequence
Eur. J. Org. Chem2010311–316 dx.doi.org/10.1002/ejoc.200901010

Sébastien Belot, Kim A. Vogt, Céline Besnard, Norbert Krause, Alexandre Alexakis
Enantioselective One-Pot Organocatalytic Michael Addition/Gold-Catalyzed Tandem Acetalyzation/Cyclization
Angew. Chem. 2009, 121, 9085-9088 dx.doi.org/10.1002/ange.200903905
Angew. Chem. Int. Ed.2009, 48, 8923–8926 dx.doi.org/10.1002/anie.200903905

Martta Asikainen, Norbert Krause
Tandem Enzyme/Gold-Catalysis: From Racemic a-Allenic Acetates to Enantiomerically Enriched 2,5-Dihydrofurans in One Pot
Adv. Synth. Catal. 2009351, 2305–2309 dx.doi.org/10.1002/adsc.200900434

Carl Deutsch, Bruce H. Lipshutz and Norbert Krause
(NHC)CuH-Catalyzed Entry to Allenes via Propargylic Carbonate SN2'-Reductions
Org. Lett. 200911, 5010–5012 dx.doi.org/10.1021/ol901868m

Yoshinari Sawama, Yuka Sawama, Norbert Krause
Highly Regioselective Gold-Catalyzed Ring-Opening Allylation and Azidation of Dihydrofurans
Org. Lett. 2009,11, 5034–5037 dx.doi.org/10.1021/ol902005e

Tomoya Miura, Masahiko Shimada, Paula de Mendoza, Carl Deutsch, Norbert Krause, Masahiro Murakami
Stereoselective Synthesis of syn-Configured a-Allenols by Rhodium-Catalyzed Reaction of Alkynyl Oxiranes with Arylboronic Acids
J. Org. Chem. 2009,74, 6050–6054 dx.doi.org/10.1021/jo900987w

Christian Winter, Norbert Krause
Structural Diversity through Gold Catalysis: Stereoselective Synthesis of N-Hydroxypyrrolines, Dihydroisoxazoles, and Dihydro-1,2-oxazines
Angew. Chem.  2009121, 6457–6460 dx.doi.org/10.1002/ange.200902355
Angew. Chem. Int. Ed200948, 6339–6342 dx.doi.org/10.1002/anie.200902355

Christian Winter, Norbert Krause
Towards Sustainable Homogeneous Gold Catalysis: Cycloisomerization of Functionalized Allenes in Water
Green Chem. 200911, 1309–1312 dx.doi.org/10.1039/b905823k

Xiaoping Tang, Simon Woodward, Norbert Krause
Synthesis of a-Hydroxyallenes by Copper-Catalyzed SN2’ Substitution of Propargylic Dioxolanones
Eur. J. Org. Chem. 2009, 2836–2844 dx.doi.org/10.1002/ejoc.200900226

Christian Winter, Norbert Krause
Rhodium(I)-Catalyzed Enantioselective C–C Bond Formation
Angew. Chem. 2009121, 2497–2499 dx.doi.org/10.1002/ange.200805578
Angew. Chem. Int. Ed200948, 2460–2462 dx.doi.org/10.1002/anie.200805578

Volker Belting, Norbert Krause
Gold-catalyzed Cycloisomerization of Alk-4-yn-1-ones
Org. Biomol. Chem20097, 1221–1225 dx.doi.org/10.1039/b819704k

Frank Volz, Sipke H. Wadman, Anja Hoffmann-Röder, Norbert Krause
Gold Catalysis in Stereoselective Natural Product Synthesis: (+)-Linalool oxide, (–)-Isocyclocapitelline, and (–)-Isochrysotricine
Tetrahedron 200965, 1902–1910 dx.doi.org/10.1016/j.tet.2008.11.104

Manojkumar Poonoth, Norbert Krause
Stereoselective Synthesis of Conjugated Bisallenols as Precursors of Novel Bis(2,5-dihydrofuran) Derivatives
Adv. Synth. Catal2009351, 117–122 dx.doi.org/10.1002/adsc.200800469

Yoshinari Sawama, Yuka Sawama, Norbert Krause
First Total Synthesis of (R,R,R)- and (3R,5S,9R)-Bejarol by Gold-catalyzed Allene Cycloisomerization and Determination of Absolute Configuration of the Natural Product
Org. Biomol. Chem. 20086, 3573–3579 dx.doi.org/10.1039/b807733a

Alexandre Alexakis, Jan E. Bäckvall, Norbert Krause, Oscar Pamies, Montserrat Diéguez
Enantioselective Copper-Catalyzed Conjugate Addition and Allylic Substitution Reactions
Chem. Rev. 2008108, 2796–2823 dx.doi.org/10.1021/cr0683515

Carl Deutsch, Norbert Krause, Bruce H. Lipshutz
CuH-Catalyzed Reactions
Chem. Rev. 2008108, 2916–2927 dx.doi.org/10.1021/cr0684321

Norbert Krause, Volker Belting, Carl Deutsch, Jörg Erdsack, Hong-Tao Fan, Birgit Gockel, Anja.Hoffmann-Röder, Nobuyoshi Morita, Frank Volz
Golden Opportunities in Catalysis
Pure Appl. Chem. 200880, 1063–1069 dx.doi.org/10.1351/pac200880051063

Özge Aksin, Norbert Krause
Gold-Catalyzed Synthesis of 2,5-Dihydrofurans in Ionic Liquids
Adv. Synth. Catal. 2008350, 1106–1112 dx.doi.org/10.1002/adsc.200800050

Nadine Bongers, Norbert Krause
Golden Opportunities in Stereoselective Catalysis
Angew. Chem. 2008120, 2208–2211 dx.doi.org/10.1002/ange.200704729​​​​​​​
Angew. Chem. Int. Ed. 200847, 2178–2181 dx.doi.org/10.1002/anie.200704729

Sandra Löhr, Jan Averbeck, Markus Schürmann, Norbert Krause
Synthesis and Complexation Properties of Allenic Bipyridines, a New Class of Axially Chiral Ligands for Transition Metal Catalysis
Eur. J. Inorg. Chem. 2008, 552 , 552–556 dx.doi.org/10.1002/ejic.200701049

Jörg Erdsack, Norbert Krause
Synthesis of Furanomycin Derivatives by Gold-Catalyzed Cycloisomerization of a-Hydroxyallenes
Synthesis 2007, 23, 3741–3750 dx.doi.org/10.1055/s-2007-990860

Manojkumar Poonoth, Markus Schürmann, Hans Preut and Norbert Krause
(2R,4S,7R,9S)-5,6-Diisopropyl-1,10-dimethoxy-3,8-dimethyldeca-3,4,6,7-tetraene-2,9-diol
Acta Cryst2007, E63, o4402

Carl Deutsch, Birgit Gockel, Anja Hoffmann-Röder, Norbert Krause
Golden Opportunities in Stereoselective Catalysis: Optimization of Chirality Transfer and Catalyst Efficiency in the Gold-Catalyzed Cycloisomerization of a-Hydroxyallenes to 2,5-Dihydrofurans
Synlett 2007, 1790–1794 dx.doi.org/10.1055/s-2007-982561

Frank Volz, Norbert Krause
Golden Opportunities in Natural Product Synthesis: First Total Synthesis of (–)-Isocyclocapitelline and (–)-Isochrysotricine by Gold-catalyzed Allene Cycloisomerization
Org. Biomol. Chem., 20075, 1519–1521 dx.doi.org/10.1039/b703995f​​​​​​​
http://www.rsc.org/Publishing/Journals/OB/News/2007/May2007/issue10.asp

Carl Deutsch, Anja Hoffmann-Röder, Axel Domke, Norbert Krause
Rapid Generation of Molecular Complexity: Synthesis of a-Hydroxyallenes Using Functionalized Grignard Reagents
Synlett 2007, 737–740. dx.doi.org/10.1055/s-2007-970768

Norbert Krause, Nobuyoshi Morita
Application of Copper, Silver and Gold in Preparative Organic Chemistry
in: “Comprehensive Organometallic Chemistry III” (R. H. Crabtree, D. M. P. Mingos, Eds.),
Elsevier, Oxford, 2007, Vol. 9, pp. 501-586 www.elsevier.com/wps/find/bookdescription.cws_home/705669/description#description

Carl Deutsch, Bruce H. Lipshutz, Norbert Krause
Small but Effective: Copper Hydride Catalyzed Synthesis of α-Hydroxyallenes
Angew. Chem. 2007119, 1677–1681 dx.doi.org/10.1002/ange.200603739​​​​​​​
Angew. Chem, Int. Ed. 200746, 1650–1653 dx.doi.org/10.1002/anie.200603739

Jörg Erdsack, Markus Schürmann, Hans Preut, Norbert Krause
tert-Butyl 2,2-dimethyl-4-(3-phenyl-2,5-dihydrofuran-2-yl)oxazolidine-3-carboxylate
Acta Cryst. 2007, o664–o665

Volker Belting, Norbert Krause
Gold-Catalyzed Tandem Cycloisomerization-Hydroalkoxylation of Homopropargylic Alcohols
Org. Lett. 20068, 4489-4492 dx.doi.org/10.1021/ol061751u

Birgit Gockel, Norbert Krause
Golden Times for Allenes: Gold-Catalyzed Cycloisomerization of β-Hydroxyallenes to Dihydropyrans
Org. Lett. 20068, 4485-4488 dx.doi.org/10.1021/ol061669z

Nobuyoshi Morita, Norbert Krause
Gold-Catalyzed Cycloisomerization of α-Aminoallenes to 3-Pyrrolines – Optimization and Mechanistic Studies
Eur. J. Org. Chem2006, 4634–4641 dx.doi.org/10.1002/ejoc.200600438

Anja Hoffmann-Röder, Norbert Krause
Efficient Synthesis of 2-Hydroxy-3,4-dienoates by Oxidation of Zirconiumallenyl Enolates with Dimethyldioxirane
Synthesis 2006, 2143-2146 dx.doi.org/10.1055/s-2006-942409

Laura Mediavilla Urbaneja, Norbert Krause
Rhodium-catalyzed Enantioselective 1,4-Additions of Arylboronic Acids to Substituted Enones
Tetrahedron: Asymmetry 2006, 17 494-496 dx.doi.org/10.1016/j.tetasy.2006.01.006

Axel Jansen, Norbert Krause
Exceptional Reactivity and Selectivity of Lower-order Cyanocuprates in the SN2'-Substitution of Propargyl Acetates
Inorg. Chim. Acta 2006 , 359, 1761-1766 dx.doi.org/10.1016/j.ica.2005.06.045

Nobuyoshi Morita, Norbert Krause
The First Gold-Catalyzed C–S Bond Formation: Cycloisomerization of α-Thioallenes to 2,5-Dihydrothiophenes
Angew. Chem2006118, 1930-1933 dx.doi.org/10.1002/ange.200503846
Angew. Chem. Int. Ed200645, 1897-1899 dx.doi.org/10.1002/anie.200503846

Jan Averbeck, Markus Schürmann, Hans Preut, Norbert Krause
6-Methyl-2-[2,2,6,6-tetramethyl-5-(2-pyridyl)hepta-3,4-dien-3-yl]pyridine
Acta Cryst. 2006E62, o951-o952 dx.doi.org/doi:10.1107/S1600536806003199

Ja.-Young. Lee, Markus Schürmann, Hans Preut,Norbert Krause
2-Methyl-4-phenylbuta-2,3-dien-1-ol
Acta Cryst. 2006, E62, o550-o551 dx.doi.org/doi:10.1107/S1600536805042960

Wolfram Henze, Armand Vyater, Norbert Krause, Ruth M. Gschwind
Influence of Tetrahydrofuran on Reactivity, Aggregation, and Aggregate Structure of Dimethylcuprates in Diethyl Ether
J. Am. Chem. Soc. 2005127, 17335-17342 dx.doi.org/10.1021/ja055085o

Seiji Mori, Marc Uerdingen, Norbert Krause, Keiji Morokuma
Elucidation of the Mechanism of the 1,6-Cuprate Addition to Acceptor-Substituted Enynes through 13C Kinetic Isotope Effects: Experimental and Theoretical Studies
Angew. Chem. Int. Ed. 200544, 4715-4719 dx.doi.org/10.1002/anie.200462976
Angew. Chem. 2005117, 4795-4798 dx.doi.org/10.1002/ange.200462976

Hong-Tao Fan, Markus Schürmann, Hans Preut, Norbert Krause
(2S,3R,4R,5R)-2-(tert-Butyldimethylsilyloxymethyl)- 2,4,5-trimethyltetrahydrofuran-3,4-diol
Acta Cryst. 2005, E61, o1987-o1988 dx.doi.org/doi:10.1107/S1600536805016831

Christian E. Janßen, Norbert Krause
Studies on the Synthesis of Macrocyclic Allenes by Ring Closing Metathesis and Doering–Moore–Skattebøl Reaction
Eur. J. Org. Chem. 2005, 2322-2329 dx.doi.org/10.1002/ejoc.200500096

Anja Hoffmann-Röder, Norbert Krause
The Golden Gate to Catalysis
Org.Biomol.Chem. 20053, 387-391 www.rsc.org/publishing/journals/OB/article.asp?doi=b416516k

Nobuyoshi Morita, Norbert Krause
Gold Catalysis in Organic Synthesis: Efficient Cycloisomerization of α-Aminoallenes to 3-Pyrrolines
Org. Lett20046, 4121-4123 dx.doi.org/10.1021/ol0481838

Norbert Krause, Anja Hoffmann-Röder
Synthesis of Allenes with Organometallic Reagents
Tetrahedron 200460, 11671-11694 dx.doi.org/10.1016/j.tet.2004.09.094

Marc Mackenstedt, Norbert Krause
Synthesis of Novel Funktionalized Polymers for the Diastereoselective Protonation of Chiral Enolates
Eur. J. Org. Chem2004, 4531-4534 dx.doi.org/10.1002/ejoc.200400429

Laura Mediavilla Urbaneja, Norbert Krause
Synthesis of Novel Bifunctional Michael Acceptors
Eur. J. Org. Chem.2004, 4467-4470 dx.doi.org/10.1002/ejoc.200400419

Claudia Zelder, Norbert Krause
Enantioselective Synthesis and Circular Dichroism of Endocyclic Allenes
Eur. J. Org. Chem2004, 3968-3971 dx.doi.org/10.1002/ejoc.200400408

Norbert Krause, A. Stephen K. Hashmi (Eds.)
Modern Allene Chemistry
Wiley-VCH, Weinheim, 2004. www.wiley-vch.de/publish/dt/books/bySubjectCH00/bySubSubjectCH50/3-527-30671-4/?sID=1

Anja Hoffmann-Röder, Norbert Krause
Metal-Mediated Synthesis of Allenes
in: „Modern Allene Chemistry“ (N. Krause, A.S.K. Hashmi, Eds.), Wiley-VCH, Weinheim, 2004, pp. 51-92 www.wiley-vch.de/publish/dt/books/bySubjectCH00/bySubSubjectCH50/3-527-30671-4/?sID=1

Norbert Krause, Anja Hoffmann-Röder
Allenic Natural Products and Pharmaceuticals
in: „Modern Allene Chemistry“ (N. Krause, A.S.K. Hashmi, Eds.), Wiley-VCH, Weinheim, 2004, pp. 997-1040 www.wiley-vch.de/publish/dt/books/bySubjectCH00/bySubSubjectCH50/3-527-30671-4/?sID=1

Norbert Krause
Funktionalisierte Allene in der Organischen Chemie: Stereoselektive Synthesen mit Kupfer, Silber und Gold
UniReport (Uni­ver­si­tät Dort­mund) 2004, 16-18Anja Hoffmann-Röder, Norbert Krause
Synthese und Eigenschaften allenischer Natur- und Wirkstoffe
Angew. Chem.2004116, 1216-1236 dx.doi.org/10.1002/ange.200300628
Angew. Chem. Int. Ed2004, 43, 1196-1216. dx.doi.org/10.1002/anie.200300628

Fritz Vögtle, Stefan Grimme, Johannes Hormes, Karl-Heinz Dötz, Norbert Krause
Strain and Chirality: Synthesis and Structure/Chiroptics-Relationships of Planar Chiral and Helical Molecules
in: „Interactions in Molecules“ (Deutsche Forschungsgemein­schaft, S.D. Peyerimhoff, Ed.),
Wiley-VCH, Weinheim, 2003, pp. 15-109 www.wiley-vch.de/publish/dt/books/ISBN3-527-27732-3/?sID=80946b3f562a8c343b19d1e3177df77b

Norbert Krause
Zum 50. Geburtstag der Organocuprate (Tagungsbericht)
Angew. Chem2003115, 393-394 dx.doi.org/10.1002/ange.200390089
(Korrektur: 873) dx.doi.org/10.1002/ange.200390195
Angew. Chem. Int. Ed. 200342, 379-380 dx.doi.org/10.1002/anie.200390121
(Correction: 849) dx.doi.org/10.1002/anie.200390226

Norbert Krause, Anja Hoffmann-Röder, Johannes Canisius
From Amino Acids to Dihydrofurans: Functionalized Allenes in Modern Organic Synthesis
Synthesis 2002, 1759-1774 dx.doi.org/10.1055/s-2002-33707

Anja Hoffmann-Röder, Norbert Krause
Enantioselektive Synthese von und mit Allenen
Angew. Chem. 2002114, 3057-3059 dx.doi.org/10.1002/1521-3757(20020816)114:16%3C3057::AID-ANGE3057%3E3.0.CO;2-S
Angew. Chem. Int. Ed. 200241, 2933-2935 dx.doi.org/10.1002/1521-3773(20020816)41:16%3C2933::AID-ANIE2933%3E3.0.CO;2-6

Axel Jansen, Norbert Krause
Transition Metal-Promoted Synthesis of Functionalized and Unfunctionalized Pyridylallenes
Synthesis 2002, 1987-1992 dx.doi.org/10.1055/s-2002-34383

Anja Hoffmann-Röder, Norbert Krause
Synthesis of Highly Functionalized Propargylic Alcohols: Direct Addition of Epoxy Acetylides to Aldehydes and Ketones
Helv. Chim. Acta 200285, 3176-3184 dx.doi.org/10.1002/1522-2675(200210)85:10%3C3176::AID-HLCA3176%3E3.0.CO;2-7

Laura Mediavilla Urbaneja, Alexandre Alexakis, Norbert Krause
Epimerization and Kinetic Resolution in Copper-catalyzed Enantioselective 1,4-Additions of Organozinc Reagents to 6-Substituted Cyclohex-2-enones
Tetrahedron Lett. 200243, 7887-7890 dx.doi.org/10.1016/S0040-4039(02)01898-1

Norbert Krause (Ed.)
Modern Organocopper Chemistry
Wiley-VCH. Weinheim, 2002 www.wiley-vch.de/publish/en/books/bySubjectCH00/bySubSubjectCH50/3-527-29773-1/?sID=5938008f9488121be26c2fb85f9b48ab%20

Norbert Krause, Anja Hoffmann-Röder
Copper-Mediated Addition and Substitution Reactions of Extended Multiple Bond Systems in:
"Modern Organocopper Chemistry" (N. Krause, Ed.), Wiley-VCH, Weinheim, 2002, pp. 145-166 www.wiley-vch.de/publish/en/books/bySubjectCH00/bySubSubjectCH50/3-527-29773-1/?sID=5938008f9488121be26c2fb85f9b48ab%20

Johannes Canisius, Markus Schürmann, Hans Preut, Norbert Krause
Crystal Structure of Ethyl (Z)-2-(acetylamino)-6,6-dimethyl-2-hepten-4-ynoate, C13H19NO3
Z. Kristallogr. NCS 2162001, 599-600.

Norbert Krause, Sophia Ebert
Synthesis of (±)-Methyl Epijasmonate and (±)-Methyl Dihydroepijasmonate by Diastereoselective Protonation 
Eur. J. Org. Chem. 2001, 3837-3841 dx.doi.org/10.1002/1099-0690(200110)2001:20%3C3837::AID-EJOC3837%3E3.0.CO;2-3

Sophia Ebert, Norbert Krause
Synthesis of the Insect Pheromone (2S,3S,7RS)-Diprionyl Acetate by Diastereoselective Protonation
Eur. J. Org. Chem. 2001, 3831-3835 dx.doi.org/10.1002/1099-0690(200110)2001:20%3C3831::AID-EJOC3831%3E3.0.CO;2-2

Anja Hoffmann-Röder, Norbert Krause
Gold(III) Chloride Catalyzed Cyclization of α-Hydroxyallenesto 2,5-Dihydrofuranes
Org. Lett. 2001, 3, 2537-2538 dx.doi.org/10.1021/ol016205+

Michael Nass, Markus Schürmann, Hans Preut,Norbert Krause
Crystal Structure of cis-Dioxobis(2,2,6,6-tetramethyl-3,5-heptandionato)-molybdenum(VI), C22H38MoO6
Z. Kristallogr. NCS 2162001, 461-464.

Johannes Canisius, T. Andrew Mobley, Stefan Berger, Norbert Krause
Mechanism of 1,6-Addition Reactions of Organocuprates:
Detailed NMR Spectroscopic Study of a Cuprate-Enyne π-Complex
Chem. Eur. J. 20017, 2671-2675 dx.doi.org/10.1002/1521-3765(20010618)7:12%3C2671::AID-CHEM26710%3E3.0.CO;2-S

Claudia Zelder, Markus Schürmann, Hans Preut, Norbert Krause
Cyclodec-2'-ynyl (1S,1'R)-(–)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylate
Acta Cryst. 2001E57, o216-o217 dx.doi.org/doi:10.1107/S1600536801002380

Norbert Krause, Anja Hoffmann-Röder
Recent Advances in Catalytic Enantioselective Michael Additions
Synthesis 2001, 171-196.
The World's Most Cited Chemistry Paper in November 2002
esi-topics.com/nhp/comments/november-02-NorbertKrause.html  dx.doi.org/10.1055/s-2001-10803

Marc Uerdingen, Markus Schürmann, Hans Preut, Norbert Krause
3,17-Dioxo-11-fluoroandrosta-4,6-diene
Acta Cryst. 2001E57, o106-o107 dx.doi.org/10.1107/S1600536801000484​​​​​​​

Norbert Krause, Martin Purpura
Remote Stereocontrol" in Organocopper Chemistry: Highly Enantioselective Synthesis of Vinylallenes by 1,5-Substitution of Enyne Acetates
Angew. Chem. 2000112, 4512-4514 dx.doi.org/10.1002/1521-3757(20001201)112:23%3C4512::AID-ANGE4512%3E3.0.CO;2-5
Angew. Chem. Int. Ed. 200039, 4355-4356 dx.doi.org/10.1002/1521-3773(20001201)39:23%3C4355::AID-ANIE4355%3E3.0.CO;2-C

Norbert Krause, Michael Laux, Anja Hoffmann-Röder
New Methods for the Stereoselective Synthesis of 2-Hydroxy-3,4-dienoates and Functionalized 2,5-Dihydrofurans 
Tetrahedron Lett. 200041, 9613-9616 dx.doi.org/10.1016/S0040-4039(00)01718-4

Norbert Krause
Copper-Catalyzed Enantioselective Michael Additions: Recent Progress with New Phosphorus Ligands
Organic Synthesis Highlights IV (Ed.: H.-G. Schmalz),
Wiley-VCH,Weinheim 2000, pp. 182-186.

Anthony L. Spek, Johannes Canisius, Hans Preut, Norbert Krause
The allyl complex di-µ-chloro-bis[(1,2,3µ)-4-oxo-5,5-dimethyl-1-(ethoxycarbonyl)hexenyl]palladium (II)
Acta Cryst. 2000C56, 1065-1066 dx.doi.org/10.1107/S0108270100008799

Marc Uerdingen, Markus Schürmann, Hans Preut, Norbert Krause
3,17- Dioxoandrosta-4,6-dien-11-yl acetate
Acta Cryst. 2000C56, e 415 dx.doi.org/10.1107/S0108270100011094

Claudia Zelder, Norbert Krause
Nucleophilic Additions to Dienes, Enynes and Polyenes, in:
The Chemistry of Dienes and Polyenes, (Ed.: Z. Rappoport),
Wiley, New York, 2000, Vol. 2, 645-691.

Marc Uerdingen, Norbert Krause
Preparative and Mechanistic Studies on Copper-Mediated 1,6-Addition Reactions to a 2,4-Dienone
Tetrahedron 200056, 2799-2804.

Johannes Canisius, Markus Schürmann, Hans Preut, Norbert Krause
Ethyl (E)-2-[benzyloxycarbonyl)amino]-6,6-dimethylhept-2-en-4-ynoate
Acta Cryst. 1999C55, IUC 9900118 dx.doi.org/10.1107/S0108270199098686

Stephan Thorand, Fritz Vögtle, Norbert Krause
Synthese des ersten [34]Allenophans: 1,3,10,12,19,21,28,30-Octamethyl-[3.3.3.3]-paracyclophan-1,2,10,11,19,20,28,29-octaen
Angew. Chem. 1999111, 3929-393
Angew. Chem. Int. Ed. 199938, 3721-3723

Stephan Thorand, Norbert Krause
Copper-Mediated 1,6-, 1,8-,1,10- and 1,12-Addition and 1,5-Substitution in Organic Synthesis
Inorg. Chim. Acta 1999296, 1-11 dx.doi.org/10.1016/S0020-1693(99)00403-X

Johannes Canisius, Andreas Gerold, Norbert Krause
The Mechanism of 1,4- and 1,6-Cuprate Additions: The First Determination of Activation Parameters
Angew. Chem. 1999111, 1727-1730 dx.doi.org/10.1002/(SICI)1521-3757(19990601)111:11%3C1727::AID-ANGE1727%3E3.0.CO;2-D
Angew. Chem. Int. Ed. 199938, 1644-1646 www3.interscience.wiley.com/cgi-bin/abstract/61501374/ABSTRACT

Norbert Krause
Selektive Organische Synthese mit Kupfer und Lithium
UniReport der Uni­ver­si­tät Dort­mund 19991, 52-55.

Martin Purpura, Norbert Krause
Regio- and Stereoselective Syntheses of Vinylallenes by 1,5-(SN´´)-Substitution of Enyne Acetates and Oxiranes with Organocuprates
Eur. J. Org. Chem. 1999, 267-275 dx.doi.org/10.1002/(SICI)1099-0690(199901)1999:1%3C267::AID-EJOC267%3E3.0.CO;2-V

Norbert Krause
New Results Regarding the Structure and Reactivity of Cyanocuprates - The End of an Old Controversy
Angew. Chem. 1999111, 83-85 dx.doi.org/10.1002/(SICI)1521-3757(19990115)111:1/2%3C83::AID-ANGE83%3E3.0.CO;2-R
Angew. Chem. Int. Ed. 199838, 79-81 dx.doi.org/10.1002/(SICI)1521-3773(19990115)38:1/2%3C79::AID-ANIE79%3E3.0.CO;2-T

Norbert Krause, Marc Mackenstedt
Preparation of the First Polymeric, Chelating Proton Donors and Their Use in Diastereoselective Protonations of Chiral Enolates
Tetrahedron Lett. 199839, 9649-9650 dx.doi.org/10.1016/S0040-4039(98)02326-0

Karolina Nilsson, Thomas Andersson, Christina Ullenius, Andreas Gerold<, Norbert Krause
NMR-Spectroscopic Investigations of the Adducts Formed by Cuprate Addition to Ynoatesand Ynones: Alkenylcuprates or Allenolates?
Chem. Eur. J. 19984, 2051-2085 www3.interscience.wiley.com/cgi-bin/abstract/5008897/ABSTRACT

Stephan Thorand, Norbert Krause
Improved Procedures for the Palladium-Catalyzed Coupling of Terminal Alkynes with Aryl Bromides (Sonogashira Coupling)
J. Org. Chem. 199863, 8551-8553.

Norbert Krause
Copper-Catalyzed Enantioselective Michael Additions: Recent Progress with New Phosphorus Ligands
Angew. Chem. 1998110, 295-297 dx.doi.org/10.1002/(SICI)1521-3757(19980202)110:3%3C295::AID-ANGE295%3E3.0.CO;2-B
Angew. Chem. Int. Ed. 199837, 283-285 www3.interscience.wiley.com/cgi-bin/abstract/10004539/ABSTRACT​​​​​​​

Norbert Krause, Sophia Ebert, Andreas Haubrich
Diastereoselective Protonation of Chiral Enolates with Chelating Proton Donors under Reagent Control: Scope, Mechanism, and Application
Liebigs Ann./Recueil 1997, 2409-2418. www3.interscience.wiley.com/cgi-bin/abstract/112377320/ABSTRACT

Michael Laux, Norbert Krause
Ruthenium-Catalyzed Flash Oxidation of Allenes to α,α´-Dihydroxyketones
Synlett 1997, 765-766. dx.doi.org/10.1055/s-1997-5759

Andreas Gerold, Johann T.B.H. Jastrzebski, Claudia M.P. Kronenburg,Norbert Krause, Gerard van Koten
Determination of the Aggregation State of Organocopper Compounds by Cryoscopy in Tetrahydrofuran
Angew. Chem. 1997109, 778-780 dx.doi.org/10.1002/ange.19971090720
Angew. Chem. Int. Ed. Engl. 199736, 755-757 dx.doi.org/10.1002/anie.199707551

Markus Becker,Norbert Krause
Allenyl Enolates - A New Class of Chiral Ambident Nucleophiles,
5. Ireland-ClaisenRearrangements of Allenic Silyl Ketene Acetals
Liebigs Ann./Recueil 1997, 725-729. www3.interscience.wiley.com/cgi-bin/abstract/112360961/ABSTRACT

Norbert Krause, Andreas Gerold
Regio- and Stereoselective Syntheses with Organocopper Reagents
Angew. Chem. 1997109, 194-213 dx.doi.org/10.1002/anie.199701861
Angew. Chem. Int. Ed. Engl. 199736, 186-204 dx.doi.org/10.1002/anie.199701861

Karolina Nilsson, Christina Ullenius, Norbert Krause
NMR Spectroscopic Evidence for π-Complexation and the Formation of a Vinylcopper Intermediate in the Reaction between
Methyl Phenylpropiolate and t-BuCu(CN)Li
J. Am. Chem. Soc. 1996118, 4194-4195 dx.doi.org/10.1021/ja953676g

Ulrich Koop, Gabriele Handke, Norbert Krause
Synthesis of Vinylallenes by Conjugate 1,6-, 1,8-, 1,10- and 1,12-Addition Reactions of Organocuprates to Acetylenic Michael Acceptors and Their Use as Dienes in Intermolecular Diels-Alder Reactions
Liebigs Ann. 1996, 1487-1499 www3.interscience.wiley.com/cgi-bin/abstract/112345690/ABSTRACT

Michael Laux,Norbert Krause, Ulrich Koop
Allenyl Enolates - A New Class of Chiral Ambident Nucleophiles,
4. Synthesis of an Enantiomerically Pure Dihydroxyester by Axis to Center Chirality Transfer
Synlett 1996, 87-88 dx.doi.org/10.1055/s-1996-5302

Norbert Krause, Michael Hohmann
Synthesis and Cycloaromatization of Enyneallenes: New Model Systems for the Neocarzinostatin Chromophore
Synlett 1996, 89-91 and 590 dx.doi.org/10.1055/s-1996-5303

Norbert Krause
Metallorganische Chemie
Selektive Synthese mit Metallorganischen Verbindungen
Spektrum Akademischer Verlag, Heidelberg, 1996 www.organic-chemistry.org/frames.htm?http://www.organic-chemistry.org/books/reviews/3860251465.shtm

Michael Hohmann, Norbert Krause
Synthesis of Allenes by 1,6-Addition of Organocuprates to Acceptor-Substituted Enynes: Scope and Limitations
Chem. Ber. 1995128, 851-860.

Norbert Krause, Gabriele Handke, Ulrich Wecker
Stereoselective 1,6-Addition Reactions of Organocuprates to Acceptor-Substituted Enynes, in:
Stereoselective Reactions of Metal-Activated Molecules
(Ed.: H. Werner, J. Sundermeyer), Vieweg, Braunschweig, 1995, pp. 153-155.

Norbert Krause, Gabriele Handke, Ulrich Wecker
Stereoselective 1,6-Addition Reactions of Organocuprates to Acceptor-Substituted Enynes, in:
Stereoselective Reactions of Metal-Activated Molecules
(Ed.: H. Werner, J. Sundermeyer), Vieweg, Braunschweig, 1995, pp. 153-155.

Norbert Krause
Substituent Effects and Complexation Phenomena in the Diastereoselective Protonation of Chiral Enolates
Angew. Chem. 1994106, 1845-1847. dx.doi%2Corg/10.1002/ange.19941061724
Angew. Chem. Int. Ed. Engl. 199433, 1764-1765 dx.doi.org/10.1002/anie.199417641

Andreas Gerold, Norbert Krause
Anti-Michael Addition of Cyanocuprate t-BuCu(CN)Li to Acceptor-Substituted Enynes
Chem. Ber. 1994127, 1547-1549.

Norbert Krause, Robert Wagner, Andreas Gerold
New Inside into the Structure of Organocuprate π-Complexes by Determination of 13C,13C- Coupling Constants
J. Am. Chem. Soc. 1994116, 381-382.

Gabriele Handke, Norbert Krause
Diastereoselective 1,6-Addition Reactions of Organocuprates to Chiral 5-Alkynylidene-1,3-dioxan-4-ones
Tetrahedron Lett. 199334, 6037-6040.

Andreas Haubrich, Mayra van Klaveren, Gerard van Koten, Gabriele Handke, Norbert Krause
1,6-Addition of Organolithium Compounds to Acceptor-Substituted Enynes Catalyzed by a Copper(I) Arenthiolate
J. Org. Chem. 199358, 5849-5852.

Norbert Krause
Synthesis of (±)-Sterpurene and Hydroxylated Derivates by 1,6-Addition of Organocuprates to Acceptor-Substituted Enynes
Liebigs Ann. Chem. 1993, 521-525. www3.interscience.wiley.com/cgi-bin/abstract/112356238/ABSTRACT

Norbert Krause
Stereoselective Conjugate Addition Reactions of Organocuprates as a Tool inOrganic Synthesis
Kontakte (Darmstadt) 1993 (1), 3-13.

Norbert Krause, Silke Arndt
Allenyl Enolates - A New Class of Chiral Ambident Nucleophiles.
2. Reaction with Iodine and Oxidizing Agents
Chem. Ber. 1993126, 261-263. dx.doi.org/10.1002/cber.19931260135

Silke Arndt, Gabriele Handke, Norbert Krause
Allenyl Enolates - A New Class of Chiral Ambident Nucleophiles.
1. Reaction with C- and Si-Electrophiles
Chem. Ber. 1993126, 251-259. dx.doi.org/10.1002/cber.19931260134

Norbert Krause
1,6- and 1,8-Addition Reactions of Organocuprates to Michael Acceptors:
NMR-Spectroscopic Observation of the Intermediates and Conclusions about the Reaction Mechanism
J. Org. Chem199257, 3509-3512.

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).