An expeditious and enantioselective entry to the ABC ring of the quassinoid skeleton

Tony K.M. Shing; Ying Tang; John F. Malone

doi:10.1039/C39890001294

An expeditious and enantioselective entry to the ABC ring of the quassinoid skeleton

Tony K.M. Shing, Ying Tang, John F. Malone

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研究成果: Article › 査読

14 被引用数 (Scopus)

抄録

The tricycle (5) with two trans-fused angular methyl groups is constructed from tiglic aldehyde and (S)-carvone involving a stereocontrolled aldol reaction and an endo-selective intramolecular Diels-Alder (IMDA) reaction; the stereochemistry was established by an X-ray study.

本文言語	English
ページ（範囲）	1294-1295
ページ数	2
ジャーナル	Journal of the Chemical Society, Chemical Communications
号	17
DOI	https://doi.org/10.1039/C39890001294
出版ステータス	Published - 1989 1月 1

ASJC Scopus subject areas

分子医療

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An expeditious and enantioselective entry to the ABC ring of the quassinoid skeleton

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