Synthesis of 2-Vinylindole-3-Acetic Acid Derivatives via Cyanide-Catalyzed Imino-Stetter Reaction

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초록

A new method for the synthesis of 2-vinyl-indole-3-acetic acid derivatives from aldimines, which are derived from 2-aminocinnamic acid derivatives and alpha,beta-unsaturated aldehydes, via a cyanide-catalyzed imino-Stetter reaction is described. Various types of 2-aminocinnamic acid derivatives and alpha,beta-unsaturated aldehydes could be used in this protocol, and the desired 2-vinyl substituted indole-3-acetic acid derivatives were obtained in high yields. This cyanide-catalyzed imino-Stetter reaction was further extended to the preparation of indole-3-acetic acid derivatives bearing a carboxylic acid functionality at the 2-position, using aldimines obtained from glyoxylates and 2-aminocinnamic acid derivatives.

키워드

INDOLE SYNTHESIS; 3-METHYL-2-VINYLINDOLES; 3-ALKYL-2-VINYLINDOLES; CONSTRUCTION; CYCLIZATION; CHEMISTRY; PROGRESS
제목
Synthesis of 2-Vinylindole-3-Acetic Acid Derivatives via Cyanide-Catalyzed Imino-Stetter Reaction
저자
Seo, Hong-Ahn; Cheon, Cheol-Hong
DOI
10.1021/acs.joc.6b01621
발행일
2016-09-02
유형
Article
저널명
The Journal of Organic Chemistry
권
81
호
17
페이지
7917 ~ 7923