Issue 22, 1970

The position of cleavage in the alkaline hydrolysis of O,S-ethylene O-methyl phosphorothioate

Abstract

O,S-Ethylene O-methyl phosphorothioate is found to undergo nucleophilic attack by hydroxide ion with P–S cleavage which contrasts with the behaviour of related cyclic O,S-esters previously reported.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1564-1565

The position of cleavage in the alkaline hydrolysis of O,S-ethylene O-methyl phosphorothioate

D. C. Gay and N. K. Hamer, J. Chem. Soc. D, 1970, 1564 DOI: 10.1039/C29700001564

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