Issue 4, 1993

Novel synthesis of substituted cis-bicyclo[3.3.0]octanes via palladium-catalysed cyclisation and subsequent Baeyer–Villiger ring cleavage

Abstract

The formal transformation of cyclopentadiene to cis-bicyclo[3.3.0]octanes via endo-5-vinyl-2-norbornene involving two different oxidation reactions, such as Pd-catalysed cyclisation and Baeyer–Villiger (BV) ring opening is described.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 420-422

Novel synthesis of substituted cis-bicyclo[3.3.0]octanes via palladium-catalysed cyclisation and subsequent Baeyer–Villiger ring cleavage

A. Heumann, S. Kaldy and A. Tenaglia, J. Chem. Soc., Chem. Commun., 1993, 420 DOI: 10.1039/C39930000420

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