A Catalyst-Free Approach to Construct 3-(Cyclopentenone)oxindoles Through a Phosphine-Ylide-Initiated Triple Domino Sequence-Reference-Cited by-同舟云学术

A Catalyst-Free Approach to Construct 3-(Cyclopentenone)oxindoles Through a Phosphine-Ylide-Initiated Triple Domino Sequence

Published:2015-04-29 Issue:7 Volume:4 Page:630-637
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Du Yanlong¹,Liu Yufen¹,Yu Aimin¹,Qin Dabin²,Zhang Kui³,Meng Xiangtai¹

Affiliation:

1. School of Chemistry&Chemical Engineering; Tianjin University of Technology; Tianjin 300384 P. R. China

2. Key Laboratory of Chemical Synthesis and Pollution Control of Sichuan Province; School of Chemistry and Chemical Engineering; China West Normal University; Nanchong 637002 P. R. China

3. Department of Chemistry and Biochemistry; University of California; Los Angeles California 90095-1569 USA

Funder

Natural Science Foundation of China

Natural Science Foundation of Tianjin

Tianjin Municipal Education Commission

Key Laboratory of Chemical Synthesis and Pollution Control of Sichuan Province

131 Talents Program of Tianjin

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajoc.201500027/fullpdf

Reference47 articles.

1. Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IκB kinase

2. Synthesis and revision of the stereochemistry of a cyclopentenone natural product isolated from ascomycete strain A23-98

3. Palladium-catalyzed tandem oxidative cyclization of 1-bromohexa-1,5-dien-3-ols: easy access to cyclopentenones

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