AuCl3 catalyzed [3 + 2 + 1] cycloaddition: first use of aldehyde as a carbon monoxide-like one carbon synthon for triple C–C coupling†
Krishnanka S. Gayen,Dilip K. Maiti
RSC Advances Pub Date : 12/19/2013 00:00:00 , DOI:10.1039/C3RA47093H
Abstract

A new [3 + 2 + 1] cycloaddition strategy is demonstrated using an aldehyde, an aldimine of a glycine ester and a terminal triple bond with AuCl3 catalyst. Aldehyde is exploited as the first alternative to the crucial partner CO for triple C–C coupled annulation for the synthesis of novel fused-tricyclic heterocycles.

Graphical abstract: AuCl3 catalyzed [3 + 2 + 1] cycloaddition: first use of aldehyde as a carbon monoxide-like one carbon synthon for triple C–C coupling