Issue 21, 1992

An efficient approach to the synthesis of 4H-1-benzothiopyran-4-ones via intramolecular Wittig reaction

Abstract

The reaction of S-acyl(aroyl)thiosalicylic acids 2 with N-phenyl(triphenylphosphoranylidene)ethenimine 3 in stepwise fashion leads to the acylphosphoranes 5 which subsequently undergo intramolecular Wittig cyclization on the thiolester carbonyl to afford the 4H-1-benzothiopyran-4-ones 7 in excellent yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 1580-1581

An efficient approach to the synthesis of 4H-1-benzothiopyran-4-ones via intramolecular Wittig reaction

P. Kumar, A. T. Rao and B. Pandey, J. Chem. Soc., Chem. Commun., 1992, 1580 DOI: 10.1039/C39920001580

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