Enantioselective Strecker-type reaction between azomethine imines and trimethylsilyl cyanide catalyzed by a cinchona alkaloid-derived thiourea bearing multiple hydrogen-bonding donors-Reference-Cited by-同舟云学术

Enantioselective Strecker-type reaction between azomethine imines and trimethylsilyl cyanide catalyzed by a cinchona alkaloid-derived thiourea bearing multiple hydrogen-bonding donors

Published:2013 Issue:24 Volume:3 Page:9154
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Li Nai-Kai,Liu Zhao-Min,Huang Xiao-Fei,Zhang Jin-Xin,Chen Xiang,Wang Yong,Wang Xing-Wang

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2013/RA/C3RA41640B

Reference59 articles.

1. Ueber die künstliche Bildung der Milchsäure und einen neuen, dem Glycocoll homologen Körper;

2. Recent Developments in Catalytic Asymmetric Strecker-Type Reactions

3. Catalytic Enantioselective Strecker Reactions and Analogous Syntheses

4. Recent Developments in the Catalytic Asymmetric Cyanation of Ketimines

5. The Catalytic Asymmetric Strecker Reaction: Ketimines Continue to Join the Fold

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