Silica gel-mediated rearrangement of allylic acetates. Application to the synthesis of 1,3-enynes

Chem Commun (Camb). 2010 Jun 21;46(23):4178-80. doi: 10.1039/c0cc00035c. Epub 2010 May 12.

Abstract

Silica gel was found to efficiently promote the rearrangement of allylic acetates into their most stable regioisomers under microwave irradiation. The reaction is easy to perform and eco-friendly. This method was applied to the metal-free synthesis of 1,3-enynes.