Issue 1, 1997

Amino Acids and Peptides. Part 48.1 Studies on the Structure of an Unexpected Reaction Product from Dipeptidyl Chloromethyl Ketone during Acid Hydrolysis 2

Abstract

During the course of the synthesis of peptidyl chloromethyl ketones (CMKs), it was revealed that amino acid recovery after acid hydrolysis (6 mol dm -3 HCl, 110 °C, 20 h) of dipeptidyl chloromethyl ketones was markedly low (7.1–33.7%) owing to the formation of 5-methylpyrazin-2(1H)-one derivatives during the acid hydrolysis.

Article information

Article type
Paper

J. Chem. Res. (S), 1997, 10-11

Amino Acids and Peptides. Part 48.1 Studies on the Structure of an Unexpected Reaction Product from Dipeptidyl Chloromethyl Ketone during Acid Hydrolysis 2

T. Yokoi, H. Taguchi, Y. Nishiyama, K. Igarashi, H. T. Y. N. K. I. F. K. Y. O., F. Kasuya and Y. Okada, J. Chem. Res. (S), 1997, 10 DOI: 10.1039/A606548A

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