Issue 4, 1999

Synthesis and stereochemical features of 2-oxo-3-cyano-1,2-thiaphosphorinanes

Abstract

The intramolecular Pishchimuka rearrangement of 3-halopropyl-substituted thiophosphorylacetonitriles results in the corresponding 2-oxo-3-cyano-1,2-thiaphosphorinanes as a statistical mixture of two diastereomers, which transforms to an individual diastereomer with time; in benzene solution, the latter turns again into an equilibrium mixture of diastereomers.

Article information

Article type
Paper

Mendeleev Commun., 1999,9, 158-160

Synthesis and stereochemical features of 2-oxo-3-cyano-1,2-thiaphosphorinanes

I. L. Odinets, N. M. Vinogradova, O. I. Artyushin, P. V. Petrovskii, K. A. Lyssenko, M. Y. Antipin and T. A. Mastryukova, Mendeleev Commun., 1999, 9, 158 DOI: 10.1070/MC1999v009n04ABEH001141

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