Lehrstuhl für
Organische Chemie I
Lichtenbergstraße 4
85747 Garching

Tel  +89.289.13330
Fax +89.289.13315

Aktuelle Publikationen
Enantioselective Lewis Acid Catalysis in Intramolecular [2+2] Photocycloaddition Reactions: A Mechanistic Comparison between Representative Coumarin and Enone Substrates
J. Am. Chem. Soc. 2015, 137, in Press
Enantioselective Template-Directed [2+2] Photocycloadditions of Isoquinolones: Scope, Mechanism and Synthetic Applications
Chem. Eur. J. 2015, 21, in Press
Enantioselective Catalysis of Photochemical Reactions (Review)
Angew. Chem. Int. Ed. 2015, 54, 3872-3890
Regioselective oxidative Pd-catalysed coupling of alkylboronic acids with pyridin-2-yl-substituted heterocycles
Chem. Commun. 2015, 51, 3166-3168
Enantiotopos-Selective CH Oxygenation Catalyzed by a Supramolecular Ruthenium Complex
Angew. Chem. Int. Ed. 2015, 54, 691-695
Stefan Kirsch

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Stefan Kirsch

Prof. Dr. rer. nat.

Bergische Universität Wuppertal
Organische Chemie
Gaußstraße 20
42119 Wuppertal

Tel.:  +49 202 439-3231

Email: eMail versenden

URL: Organische Chemie - Bergische Universität Wuppertal

6. S. F. Kirsch, T. Bach, Chem. Eur. J. 2005, 11, 7007-7023.
'Diastereoselective Reactions at Enantiomerically Pure, Sterically Congested Cyclohexanes as an Entry to Wailupemycins A and B. Total Synthesis of (+)-Wailupemycin B'
Forschungsgebiet: Wailupemycin B
Artikel: → Link zum Artikel
5. S. Kirsch, T. Bach, Synthesis 2005, 2657-2660.
'Chiral 2,4,6-Trihydroxycyclohexanones as Potent Building Blocks: A Convenient Method for the Preparation of Enantiomerically Pure Acyclic 1,3-Diols'
Forschungsgebiet: Wailupemycin B
Artikel: → Link zum Artikel
4. S. Kirsch, O. Ackermann, K. Harms, T. Bach, Monatsh. Chem. 2004, 135, 713-727.
'Regioselective Isomerisation of Highly Substituted 1-Methylenecyclohexenepoxides to the Corresponding Allylic Alcohols. Influence of the Base and of the Protecting Groups'
Forschungsgebiet: Wailupemycin B
Artikel: → Link zum Artikel
3. S. Kirsch, T. Bach, Synthesis 2003, 1827-1836.
'Stereoselective Synthesis of Enantiomerically Pure, Orthogonally Protected 2,4,6-Trihydroxycyclohexanones and 2-Methylenecyclohexan-1,3,5-triols'
Forschungsgebiet: Wailupemycin B
Artikel: → Link zum Artikel
2. S. Kirsch, T. Bach, Angew. Chem. Int. Ed. 2003, 42, 4685-4687; Angew. Chem. 2003, 115, 4833-4835.
'Total Synthesis of (+)-Wailupemycin B'
Forschungsgebiet: Wailupemycin B
Artikel: → Link zum Artikel
1. T. Bach, S. Kirsch, Synlett 2001, 1974-1976.
'Synthesis of 6-Substituted 4-Hydroxy-2-pyrones from Aldehydes by Addition of an Acetoacetate Equivalent, Oxidation and Subsequent Cyclization'
Forschungsgebiet: Wailupemycin B
Artikel: → Link zum Artikel