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

Tony Kung Ming Shing; Ying Tang; John F. Malone

doi:10.1039/C39890001294

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

Tony Kung Ming Shing, Ying Tang, John F. Malone

Research output: Contribution to journal › Article

14 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	1294-1295
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	17
DOIs	https://doi.org/10.1039/C39890001294
Publication status	Published - 1989 Jan 1
Externally published	Yes

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ASJC Scopus subject areas

Molecular Medicine

Cite this

Shing, T. K. M., Tang, Y., & Malone, J. F. (1989). An expeditious and enantioselective entry to the ABC ring of the quassinoid skeleton. Journal of the Chemical Society, Chemical Communications, (17), 1294-1295. https://doi.org/10.1039/C39890001294

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Access to Document

10.1039/C39890001294