The design of a spiro-pyrrolidine organocatalyst and its application to catalytic asymmetric Michael addition for the construction of all-carbon quaternary centers-Reference-Cited by-同舟云学术

The design of a spiro-pyrrolidine organocatalyst and its application to catalytic asymmetric Michael addition for the construction of all-carbon quaternary centers

Published:2015 Issue:49 Volume:51 Page:9979-9982
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Tian Jin-Miao¹²³⁴,Yuan Yong-Hai¹²³⁴,Tu Yong-Qiang¹²³⁴⁵,Zhang Fu-Min¹²³⁴,Zhang Xiao-Bo¹²³⁴,Zhang Shi-Heng¹²³⁴,Wang Shao-Hua¹²³⁴,Zhang Xiao-Ming¹²³⁴

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry & College of Chemistry and Chemical Engineering

2. Lanzhou University

3. Lanzhou

4. P. R. China

5. Collaborative Innovation Center of Chemical Science and Engineering

Abstract

A novel chiral spiro-pyrrolidine silyl ether organocatalyst has been designed and applied to an asymmetric Michael addition reaction.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CC/C5CC02765A

Reference69 articles.

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2. H. Pellissier , Recent Developments in Asymmetric Organocatalysis, Royal Society of Chemistry, 2010

3. Asymmetric Enamine Catalysis

4. Iminium Catalysis

5. Asymmetric Aminocatalysis-Gold Rush in Organic Chemistry

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