Silver-Catalyzed Asymmetric Desymmetrization of Cyclopentenediones via [3 + 2] Cycloaddition with α-Substituted Isocyanoacetates

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29
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SCOPUS

30

초록

A highly selective and practical asymmetric Ag(I) catalyst system has been developed for the [3 + 2] cycloaddition reactions between isocyanoacetates and cyclopentenediones. The current Ag(I) catalyst system tolerates moisture and air and readily utilizes class III solvents such as EtOAc and acetone. The development of on demand generation of an active chiral catalyst in the presence of isocyanides paves a way to the efficient asymmetric preparation of bicyclic pyrrolidines with four stereogenic centers, including two quaternary centers in 80-97% ee.

키워드

ENANTIOSELECTIVE VINYLOGOUS MANNICH; CARBON QUATERNARY STEREOCENTERS; ALDOL REACTION; BINAP-CENTER-DOT-SILVER(I) COMPLEX; BICYCLIC PYRROLIDINES; ALKYNYL IMINES; ARYL KETONES; ALDEHYDES; EFFICIENT; ISOCYANIDES
제목
Silver-Catalyzed Asymmetric Desymmetrization of Cyclopentenediones via [3 + 2] Cycloaddition with α-Substituted Isocyanoacetates
저자
George, Jimil; Kim, Hun Young; Oh, Kyungsoo
DOI
10.1021/acs.orglett.8b00590
발행일
2018-04
유형
Article
저널명
Organic Letters
권
20
호
8
페이지
2249 ~ 2252