Issue 22, 1975

Micellar control of the rate and stereochemical course of the hydrolysis of 1-methylheptyl trifluoromethanesulphonate

Abstract

Hydrolytic alkyl–oxygen bond fission of optically active 1-methylheptyl trifluoromethanesulphonate is extensively retarded by micelles of cetyltrimethyl-ammonium bromide and sodium lauryl sulphate and proceeds with predominant retention of configuration.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 922-923

Micellar control of the rate and stereochemical course of the hydrolysis of 1-methylheptyl trifluoromethanesulphonate

K. Okamoto, T. Kinoshita and H. Yoneda, J. Chem. Soc., Chem. Commun., 1975, 922 DOI: 10.1039/C39750000922

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