Intramolecular PIFA-mediated alkyne amidation and carboxylation reaction

J Org Chem. 2007 Feb 16;72(4):1526-9. doi: 10.1021/jo062320s.

Abstract

The hypervalent iodine reagent PIFA promotes the intramolecular electrophilic cyclization of easily accessible alkynylamides and alkynyl carboxylic acids, leading to the formation of pyrrolidinone and lactone skeletons, respectively, in a very efficient way. A synthetic study and a mechanistic proposal for these transformations are presented.