Sterically and Electronically Tunable and Bifunctional Organocatalysts: Design and Application in Asymmetric Aldol Reaction of Cyclic Ketones with Aldehydes-Reference-Cited by-同舟云学术

Sterically and Electronically Tunable and Bifunctional Organocatalysts: Design and Application in Asymmetric Aldol Reaction of Cyclic Ketones with Aldehydes

Published:2006-09-15 Issue:21 Volume:71 Page:8198-8202
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chen Jia-Rong¹,Li Xin-Yong¹,Xing Xiao-Ning¹,Xiao Wen-Jing¹

Affiliation:

1. Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0615089

Reference49 articles.

1. Kim, B. M.; Williams, S. F.; Masamune, S. InComprehensive OrganicSynthesis; Trost, B. M., Fleming, I., Heathcock, C. H., Eds.; Pergamon: Oxford, 1991; Vol. 2, p 229.

2. The Efficient Catalytic Asymmetric Aldol-type Reaction

3. New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride

4. New Catalytic Concepts for the Asymmetric Aldol Reaction

5. Asymmetrische Katalyse mit Hetero-Dimetall-Verbindungen

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