Issue 2, 1972

Stereochemistry of the acetalization of hexafluoroacetone with a bromohydrin

Abstract

Acetalization of hexafluoroacetone with threo- and erythro-5-bromo-octan-4-ol has been shown to be highly trans-specific by 19F n.m.r., providing a method for establishing the stereochemistry of bromohydrins and their precursors when they are reacted stereospecifically.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 99-100

Stereochemistry of the acetalization of hexafluoroacetone with a bromohydrin

B. M. Johnson and J. W. Taylor, J. Chem. Soc., Chem. Commun., 1972, 99 DOI: 10.1039/C39720000099

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