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Diastereotopic group selective intramolecular cycloadditions of sulfenic acids to 1,4-dienes†
Richard S. Grainger,Patrizia Tisselli,Jonathan W. Steed
Organic & Biomolecular Chemistry Pub Date : 12/01/2003 00:00:00 , DOI:10.1039/B314176D
Abstract

The ratio of diastereomeric cis-fused perhydrobenzothiophene S-oxides formed via the intramolecular addition of a sulfenic acid to a 1,4-diene is controlled by the nature of the protecting group on a chiral alcohol in the connecting chain.

Graphical abstract: Diastereotopic group selective intramolecular cycloadditions of sulfenic acids to 1,4-dienes
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