Issue 12, 1993

A revised mechanism for the cycioaddition of mesoionic dithioles with heterocumulenes

Abstract

The reaction of a mesoionic 1,3-dithiolium-4-olate with phenyl isocyanate is not a 1,3-dipolar cycloaddition as the primary cycloadduct is an azetidinedione which probably results from the addition of phenyl isocyanate with the opened ketene form of the mesoionic compound.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 998-999

A revised mechanism for the cycioaddition of mesoionic dithioles with heterocumulenes

M. Bssaibis, A. Roberf and A. Souizi, J. Chem. Soc., Chem. Commun., 1993, 998 DOI: 10.1039/C39930000998

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