A highly organocatalytic stereoselective double Michael reaction: efficient construction of optically enriched spirocyclic oxindoles-Reference-Cited by-同舟云学术

A highly organocatalytic stereoselective double Michael reaction: efficient construction of optically enriched spirocyclic oxindoles

Published:2011 Issue:19 Volume:47 Page:5593-5595
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wang Liang-Liang¹²³⁴⁵,Peng Lin¹²³⁴⁵,Bai Jian-Fei¹²³⁴⁵,Jia Li-Na¹²³⁴⁵,Luo Xi-Ya¹²³⁴⁵,Huang Qing-Chun¹²³⁴⁵,Xu Xiao-Ying¹²³⁴⁵,Wang Li-Xin¹²³⁴⁵

Affiliation:

1. Key Laboratory of Asymmetric Synthesis and Chirotechnology of Sichuan Province

2. Chengdu Institute of Organic Chemistry

3. Chinese Academy of Sciences

4. Chengdu 610041

5. China

Abstract

An array of spirocyclic oxindoles have been constructed via a double Michael reaction in high yields and excellent enantioselectivities.

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/2011/CC/C1CC11223F

Reference34 articles.

1. In the Golden Age of Organocatalysis

2. The advent and development of organocatalysis

3. Asymmetric Organocatalysis: From Infancy to Adolescence

4. Asymmetric Aminocatalysis-Gold Rush in Organic Chemistry

5. Organocatalysis—after the gold rush

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