Issue 17, 1989

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

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1294-1295

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

T. K. M. Shing, Y. Tang and J. F. Malone, J. Chem. Soc., Chem. Commun., 1989, 1294 DOI: 10.1039/C39890001294

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