Highly enantioselective synthesis of warfarin and its analogs by means of cooperative LiClO4/DPEN-catalyzed Michael reaction: enantioselectivity enhancement and mechanism-Reference-Cited by-同舟云学术

Highly enantioselective synthesis of warfarin and its analogs by means of cooperative LiClO4/DPEN-catalyzed Michael reaction: enantioselectivity enhancement and mechanism

Published:2010-12 Issue:51 Volume:66 Page:9708-9713
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Yang Hua-Meng,Li Li,Jiang Ke-Zhi,Jiang Jian-Xiong,Lai Guo-Qiao,Xu Li-Wen

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference50 articles.

1. Selected recent reviews, see:

2. The oxa-Michael reaction: from recent developments to applications in natural product synthesis

3. Recent Advances in Metal-Catalyzed Asymmetric Conjugate Additions

4. The Phospha‐Michael Addition in Organic Synthesis

5. A Catalytic Enantioselective Aza‐Michael Reaction: Novel Protocols for Asymmetric Synthesis of β‐Amino Carbonyl Compounds

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