An efficient and enantioselective Michael addition of aromatic oximes to α ,β -unsaturated aldehydes promoted by a chiral diamine catalyst derived from α ,α -diphenyl prolinol-Reference-Cited by-同舟云学术

An efficient and enantioselective Michael addition of aromatic oximes to α ,β -unsaturated aldehydes promoted by a chiral diamine catalyst derived from α ,α -diphenyl prolinol

Published:2017-04-18 Issue:7 Volume:29 Page:369-375
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Chen Feng¹²^ORCID,Ren Hong-Xia¹²,Yang Yu¹²,Ji Shan-Ping¹²,Zhang Zheng-Bing¹²,Tian Fang¹,Peng Lin¹,Wang Li-Xin¹

Affiliation:

1. Key Laboratory of Asymmetric Synthesis and Chirotechnology of Sichuan Province; Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences; Chengdu China

2. University of Chinese Academy of Sciences; Beijing China

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

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4. Natural products as inspiration for the development of asymmetric catalysis;Mohr;Nature,2008

5. Organocatalysis--after the gold rush;Bertelsen;Chem Soc Rev,2009

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1. Asymmetric Michael Addition of Isobutyraldehyde to Nitroolefins Using an α,α-Diphenyl-(S)-prolinol-Derived Chiral Diamine Catalyst;Bulletin of the Chemical Society of Japan;2020-08-15

2. Three-Component Multi-Catalytic Enantioselective Oxa-Michael/Aldolization Sequence and Application to (+)-Yashabushitriol Synthesis;European Journal of Organic Chemistry;2020-03-05

3. Theoretical study on the reaction mechanisms of Michael chirality addition between propionaldehyde and nitroalkene catalyzed by an enantioselective catalyst;Chirality;2018-04-02