Issue 23, 1979

Stereochemistry of methylcyclohexanones reduction by sodium dithionite under conventional and phase transfer conditions

Abstract

Reduction of methylcyclohexanones by sodium dithionite in benzene–water using Adogen as the phase transfer agent affords good yields of isomeric mixtures of the corresponding methylcyclohexanols with stereoselectivities comparable to those exhibited by conventional hydride reagents.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 1080-1081

Stereochemistry of methylcyclohexanones reduction by sodium dithionite under conventional and phase transfer conditions

F. Camps, J. Coll and M. Riba, J. Chem. Soc., Chem. Commun., 1979, 1080 DOI: 10.1039/C39790001080

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