On the Structure of Intermediates in Enyne Gold(I)‐Catalyzed Cyclizations: Formation of <i>trans</i>‐Fused Bicyclo[5.1.0]octanes as a Case Study

Abstract

The nature of cyclopropyl gold(I) carbene-type intermediates has been reexamined as part of a mechanistic study on the formation of cis- or trans-fused bicyclo[5.1.0]octanes in a gold(I)-catalyzed cascade reaction. Benchmark of DFT methods together with QTAIM theory and NBO analysis confirms the formation of distinct intermediates with carbenic or carbocationic structures in the cycloisomerizations of enynes.