A stereocontrolled and enantioselective synthesis of the tetracyclic quassinoid skeleton

Tony K.M. Shing; Ying Tang

doi:10.1039/C39920000341

A stereocontrolled and enantioselective synthesis of the tetracyclic quassinoid skeleton

Tony K.M. Shing, Ying Tang

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

12 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 language	English
Pages (from-to)	341-342
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	4
DOIs	https://doi.org/10.1039/C39920000341
Publication status	Published - 1992 Dec 1

ASJC Scopus subject areas

Molecular Medicine

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title = "A stereocontrolled and enantioselective synthesis of the tetracyclic quassinoid skeleton",

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.",

author = "Shing, {Tony K.M.} and Ying Tang",

year = "1992",

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journal = "Chemical Communications",

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N2 - 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.

AB - 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.

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A stereocontrolled and enantioselective synthesis of the tetracyclic quassinoid skeleton

Abstract

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