Issue 0, 1985

Application of diphenylphosphinic carboxylic mixed anhydrides to peptide synthesis

Abstract

Diphenylphosphinic carboxylic mixed anhydrides formed in situ from Nα-protected amino acids and diphenylphosphinic chloride have been critically evaluated in peptide synthesis. Wherever possible, 32.4 MHz 31P n.m.r. spectroscopy has been employed to follow the rates of both mixed anhydride formation and aminolysis.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1985, 461-470

Application of diphenylphosphinic carboxylic mixed anhydrides to peptide synthesis

R. Ramage, D. Hopton, M. J. Parrott, R. S. Richardson, G. W. Kenner and G. A. Moore, J. Chem. Soc., Perkin Trans. 1, 1985, 461 DOI: 10.1039/P19850000461

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