Asymmetric synthesis of (2-carbamoyloxy-1-alkenyl)cyclopropanes by intramolecular cycloalkylation

Enantioenriched, diastereomerically pure (2-carbamoyloxy-1-alkenyl)cyclopropanes are easily prepared via deprotonation of different allyl carbamates with n-butyllithium and (−)-sparteine (). The mechanism of the cyclization reaction was determined and several substituted (S)-configured vinylcyclopropanes were synthesized by two different methods. The configurational stability of the intermediate lithiated allyl carbamates and the half-time of epimerization were investigated in a series of silylation experiments, achieving up to 90% ee in the kinetically controlled enantiotopos-differentiating deprotonation.