Issue 2, 1978

New method for reduction of ketones and primary alcohols to hydrocarbons: reaction of the derived selenides with tin hydrides

Abstract

Phenyl selenides and selenoacetals are reduced by triphenyltin hydride in a process that constitutes an efficient method for hydrogenolysis of ketone C[double bond, length half m-dash]O and primary alcohol C–OH bonds.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 41-42

New method for reduction of ketones and primary alcohols to hydrocarbons: reaction of the derived selenides with tin hydrides

D. L. J. Clive, G. Chittattu and C. K. Wong, J. Chem. Soc., Chem. Commun., 1978, 41 DOI: 10.1039/C39780000041

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