Abstract The potential application of 1-oxo-1-chlorophospholane (5) as a novel reagent for the in situ activation of Nα-protected amino acids for use in peptide bond forming reactions has been examined. Wherever possible, 32.4 Mhz 31 P nuclear magnetic resonance (nmr) spectroscopy was employed to follow both the formation of the intermediate phospholanic- carboxylic mixed anhydride and the subsequent aminolysis reaction.
[Ramage, Robert; Atrash, Butrus; Hopton, David; Parrott, Maxwell J. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985 , p. 1617 - 1622]