Expeditious and enantiospecific avenue to pentacyclic quassinoid skeleton

Tony K.M. Shing; Xue Y. Zhu; Thomas C.W. Mak

doi:10.1039/cc9960002369

Expeditious and enantiospecific avenue to pentacyclic quassinoid skeleton

Tony K.M. Shing, Xue Y. Zhu, Thomas C.W. Mak

Department of Chemistry

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

9 Citations (Scopus)

Abstract

The pentacyclic quassinoid skeleton 3 is constructed from (S)-carvone involving a 1,3-sigmatropic rearrangement and an intramolecular Diels-Alder reaction as the key steps.

Original language	English
Pages (from-to)	2369-2370
Number of pages	2
Journal	Chemical Communications
Issue number	20
DOIs	https://doi.org/10.1039/cc9960002369
Publication status	Published - 1996 Jan 1

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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title = "Expeditious and enantiospecific avenue to pentacyclic quassinoid skeleton",

abstract = "The pentacyclic quassinoid skeleton 3 is constructed from (S)-carvone involving a 1,3-sigmatropic rearrangement and an intramolecular Diels-Alder reaction as the key steps.",

author = "Shing, {Tony K.M.} and Zhu, {Xue Y.} and Mak, {Thomas C.W.}",

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