Regio- and diastereoselective conjugate addition of Grignard reagents to aryl substituted α,β-unsaturated carbonyl compounds derived from Oppolzer's sultam-Reference-Cited by-同舟云学术

Regio- and diastereoselective conjugate addition of Grignard reagents to aryl substituted α,β-unsaturated carbonyl compounds derived from Oppolzer's sultam

Published:2008-06 Issue:24 Volume:64 Page:5629-5636
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Cao Xiufang,Liu Fang,Lu Wenchang,Chen Gang,Yu Guang-Ao,Liu Sheng Hua

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference51 articles.

1. Conjugate Addition Reactions in Organic Synthesis;Perlmutter,1992

2. Asymmetric conjugate addition

3. Diastereoselective conjugate addition of Grignard reagents to a homochiral fumaramide derived from Oppolzer’s sultam

4. On the Mechanism of the Copper-Catalyzed Enantioselective 1,4-Addition of Grignard Reagents to α,β-Unsaturated Carbonyl Compounds

5. Reactions of carbonyl compounds with Grignard reagents in the presence of cerium chloride

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