Synthesis of Benzo[a]quinolizidines via an Aza-Michael/Oxidative Mannich Process

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초록

The synthesis of substituted benzo[a]quinolizidines via aza-Michael addition of tetrahydroisoquinolines to alkyl vinyl ketones, followed by oxidative Mannich cyclization, is described. Various Michael adducts are easily prepared, and subsequent DDQ-mediated oxidations stereoselectively afford the corresponding azacycles efficiently. Furthermore, the one-pot aza-Michael/oxidative Mannich process gave benzo[a]quinolizidines, thus providing a metal-free and practical synthetic route to N-heterocyclic building blocks.

키워드

aza-Michaelsynthetic methodscyclizationoxidative Mannich reactionbenzo[a]quinolizidinesSTEREOCONTROLLED SYNTHESISASYMMETRIC-SYNTHESISCYCLIC IMINESTETRABENAZINE(-)-EMETINECONSTRUCTIONPROTOEMETINECYCLIZATIONSDERIVATIVESSTRATEGY
제목
Synthesis of Benzo[a]quinolizidines via an Aza-Michael/Oxidative Mannich Process
저자
Jung, AreumMin, Sun-Joon
DOI
10.1002/ajoc.201900137
발행일
2019-09
유형
Article
저널명
Asian Journal of Organic Chemistry
8
9
페이지
1617 ~ 1620