A One-Pot Synthesis of Pyranone and Pyrrole Derivatives from β-Chlorovinyl Ketones via Direct Conjugate Addition Approach

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WEB OF SCIENCE

22
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SCOPUS

21

초록

The direct conjugate addition reactions of imino esters to β-chlorovinyl ketones have been accomplished in the presence of a substoichiometric amount of hard base, LiHMDS. An in situ generated species from the conjugate addition reaction readily acted as autocatalyst to convert the imino esters to its corresponding enolates. By utilizing a sequence of conjugate addition/elimination/lactonization followed by either reduction or reaction with amines, the novel one-pot syntheses of highly functionalized pyranone and pyrrole derivatives were accomplished in good to excellent yields.

키워드

VINYL ENOLIZATION STRATEGY; (E)-BETA-CHLOROVINYL KETONES; ASYMMETRIC-SYNTHESIS; ALKYNES; ACIDS; PATHWAYS; SEQUENCE; ALLENYL; ANION
제목
A One-Pot Synthesis of Pyranone and Pyrrole Derivatives from β-Chlorovinyl Ketones via Direct Conjugate Addition Approach
저자
Kim, Hun Young; Oh, Kyungsoo
DOI
10.1021/acs.orglett.7b02381
발행일
2017-09
유형
Article
저널명
Organic Letters
권
19
호
18
페이지
4904 ~ 4907