Reversed Stereochemical Course of theMichael Addition of Cyclohexanone to ?-Nitrostyrenes by Using 1-(Trimethylsiloxy)cyclohexene/Dichloro(diisopropoxy)titanium. Preliminary Communication-Reference-Cited by-同舟云学术

Reversed Stereochemical Course of theMichael Addition of Cyclohexanone to ?-Nitrostyrenes by Using 1-(Trimethylsiloxy)cyclohexene/Dichloro(diisopropoxy)titanium. Preliminary Communication

Published:1985-03-27 Issue:2 Volume:68 Page:319-324
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Seebach Dieter,Brook Michael A.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference53 articles.

1. Synthesis of Open-Chain 2,3-Disubstituted 4-nitroketones by DiastereoselectiveMichael-addition of (E)-Enamines to (E)-Nitroolefins. A topological rule for C, C-bond forming processes between prochiral centres. Preliminary communication

2. 2, 3-Disubstituted γ-Butyrolactams from theMichael-Additions of Doubly Deprotonated, Optically Active β-Hydroxycarboxylates to Nitroolefins. Preliminary Communication

3. Über den sterischen Verlauf der Umsetzung von Enaminen aus offenkettigen Aldehyden und Ketonen mit Nitroolefinen zu 2,3-disubstituierten 4-Nitroketonen

4. (c) unpublished results.

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