Aminolysis of Activated Esters Formed by Reaction of Carboxylate Salts with Strained Phosphonates and Phosphinates

Abstract
Nucleophilic attack of a carboxylate salt on a five-membered phosphonic or phosphinic ester followed by an intramolecular acyl transfer reaction gives a substituted aryl ester. Due to the intramolecular base catalysis of a neighbouring P=O group the bimolecular aminolysis of this ester is a fast process.

This publication has 1 reference indexed in Scilit: