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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
22Citations
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21초록
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
- 발행일
- 2017-09
- 유형
- Article
- 저널명
- Organic Letters
- 권
- 19
- 호
- 18
- 페이지
- 4904 ~ 4907
- 언어
- ENG
- 출판사
- AMER CHEMICAL SOC
- 발행국가
- 미국
- 분량
- 4 페이지
- ISSN
- E 1523-7052
P 1523-7060