Issue 22, 1972

Reaction of chlorosulphonyl isocyanate with cyclic dienes. Evidence for a true dipole in 2 + 2 addition

Abstract

The first reactions of chlorosulphonyl isocyanate with cyclohexadienes involve primary addition to yield N-chlorosulphonyl β-lactams followed by secondary and tertiary dipolar rearrangements; evidence for the intermediacy of a true dipole in β-lactam formation is presented.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1247-1248

Reaction of chlorosulphonyl isocyanate with cyclic dienes. Evidence for a true dipole in 2 + 2 addition

J. R. Malpass and N. J. Tweddle, J. Chem. Soc., Chem. Commun., 1972, 1247 DOI: 10.1039/C39720001247

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