Wang S S, Kulesha I D, Winter D P, Makofske R, Kutny R, Meienhofer J
Int J Pept Protein Res. 1978 Apr;11(4):297-300. doi: 10.1111/j.1399-3011.1978.tb02852.x.
A mild procedure for preparing protected peptide hydrazides directly from the corresponding carboxylic acids and equivalent amounts of hydrazine, N-hydroxybenzotriazole and dicyclohexylcarbodiimide is described. Side reactions frequently encountered in hydrazinolysis are thus totally avoided. The process is especially useful for the preparation of aspartic acid and glutamic acid containing peptide hydrazides. No racemization of the amino acid residue was observed.
本文描述了一种温和的方法,可直接从相应的羧酸与等量的肼、N-羟基苯并三唑和二环己基碳二亚胺制备保护肽酰肼。由此完全避免了肼解反应中经常遇到的副反应。该方法对于制备含天冬氨酸和谷氨酸的肽酰肼特别有用。未观察到氨基酸残基的消旋化。