Intramolecular Fischer Indole Synthesis for the Direct Synthesis of 3,4-Fused Tricyclic Indole and Application to the Total Synthesis of (-)-Aurantioclavine

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초록

Aryl hydrazides with a ketone or aldehyde containing side chains linked to the meta-position of the aromatic ring undergo acid-promoted intramolecular Fischer indole synthesis to generate 3,4-fused tricyclic indoles. The preparative utility of this conceptually new synthetic approach, which does not require prefunctionalization of the indole ring, was demonstrated by its application to a concise total synthesis of (-)-aurantioclavine.

키워드

(-)-N-METHYLWELWITINDOLINONE C ISONITRILE; ALLYLIC AMINATION; (+/-)-WELWITINDOLINONE-A ISONITRILE; (-)-COMMUNESIN F; ALKALOIDS; (+/-)-AURANTIOCLAVINE; HYDROARYLATION; COMBINATION; ANNULATION; ALCOHOLS
제목
Intramolecular Fischer Indole Synthesis for the Direct Synthesis of 3,4-Fused Tricyclic Indole and Application to the Total Synthesis of (-)-Aurantioclavine
저자
Park, Jun; Kim, Dong-Hyun; Das, Tapas; Cho, Cheon-Gyu
DOI
10.1021/acs.orglett.6b02541
발행일
2016-10
유형
Article
저널명
Organic Letters
권
18
호
19
페이지
5098 ~ 5101