Issue 11, 1974

Extension of the “handle” method of peptide synthesis: the use of 4-picolyloxycarbonylhydrazides

Abstract

The 4-picolyloxycarbonylhydrazide of a carboxy-terminal amino-acid [e.g.(I)] provides a weakly basic ‘handle’ by which the coupling product can readily be isolated at each stage of peptide synthesis; then hydrogenolysis of the 4-picolyl group yields the hydrazide required for fragment coupling.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 446-447

Extension of the “handle” method of peptide synthesis: the use of 4-picolyloxycarbonylhydrazides

R. Macrae and G. T. Young, J. Chem. Soc., Chem. Commun., 1974, 446 DOI: 10.1039/C39740000446

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