A stereocontrolled and enantioselective synthesis of the tetracyclic quassinoid skeleton

Tony Kung Ming Shing, Ying Tang

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

The optically active tetracycle 2 with six correct chiral centres common to numerous quassinoids is constructed from (S)-carvone and 3-methyl-2,5- dihydrothiophene S,S-dioxide involving highly regioselective and stereocontrolled reactions.

Original languageEnglish
Pages (from-to)341-342
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number4
DOIs
Publication statusPublished - 1992 Dec 1
Externally publishedYes

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Quassins
Skeleton
carvone

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

A stereocontrolled and enantioselective synthesis of the tetracyclic quassinoid skeleton. / Shing, Tony Kung Ming; Tang, Ying.

In: Journal of the Chemical Society, Chemical Communications, No. 4, 01.12.1992, p. 341-342.

Research output: Contribution to journalArticle

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