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.
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