Organocatalytic Direct Asymmetric Aldol Reactions of 3-Isothiocyanato Oxindoles to Ketones: Stereocontrolled Synthesis of Spirooxindoles Bearing Highly Congested Contiguous Tetrasubstituted Stereocenters-Reference-Cited by-同舟云学术

Organocatalytic Direct Asymmetric Aldol Reactions of 3-Isothiocyanato Oxindoles to Ketones: Stereocontrolled Synthesis of Spirooxindoles Bearing Highly Congested Contiguous Tetrasubstituted Stereocenters

Published:2011-04-07 Issue:9 Volume:13 Page:2472-2475
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chen Wen-Bing¹²³,Wu Zhi-Jun¹²³,Hu Jing¹²³,Cun Lin-Feng¹²³,Zhang Xiao-Mei¹²³,Yuan Wei-Cheng¹²³

Affiliation:

1. Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, China

2. Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China

3. Graduate School of Chinese Academy of Sciences, Beijing 100049, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol200724q

Reference61 articles.

1. aModern Aldol Reactions;Mahrwald, R., Ed.Wiley-VCH:Weinheim, Germany, 2004; Vol.1, p2.

2. Catalyzed enantioselective aldol additions of latent enolate equivalents

3. Current progress in the asymmetric aldol addition reaction

4. Recent Advances in Aldolase-Catalyzed Asymmetric Synthesis

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