Issue 4, 1987

A simple synthesis of cis- and trans-fused 14,15-dinoreudesmanolides

Abstract

Three possible stereoisomers of 14,15-dinoreudesmanolide, the structure of which consists of an α-methylene-γ-lactone ring fused to a trans-decalin ring, have been synthesized from a dialdehyde monoacetal viaα-trimethylsilylmethyl-α,β-unsaturated esters.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 286-288

A simple synthesis of cis- and trans-fused 14,15-dinoreudesmanolides

C. Kuroda, S. Shimizu and J. Y. Satoh, J. Chem. Soc., Chem. Commun., 1987, 286 DOI: 10.1039/C39870000286

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