Conrotatory ring-opening reactions of cyclopropyl anions in monocyclic and tricyclic systems

Org Lett. 2004 Mar 18;6(6):901-4. doi: 10.1021/ol036448x.

Abstract

[reaction: see text] Only conrotatory transition structures were located by B3LYP6-311++G(3df, 2p) computations for the electrocyclic ring opening of cyclopropyl anions having different substituents (H, Me, CN). The transition structure for the similarly substituted cyclopropyl anion fused to a bicyclic system exhibits the same features, in apparent contradiction with the observed product. A reaction path where the direction of twist changes after the transition state provides an explanation alternative to those proposed in recent reports.