Synthesis of diastereomers of sarcolysylleucine

Autor: O. V. Kil'disheva, R. B. Klyukene, K. I. Karpavichyus
Rok vydání: 1978
Předmět:
Zdroj: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:622-624
ISSN: 1573-9171
0568-5230
DOI: 10.1007/bf00923961
Popis: 1. The diastereomers of sarcolysylleucine with a formylated and free amino group in sarcolysine residue were obtained by using the N-ethoxycarbonyl-2-ethoxy-1, 2-dihydroquinoline method to form the peptide linkage. 2. The possibility of deformylating peptides, containing the di-2-chloroethyl group, by hydrazine acetate was studied.
Databáze: OpenAIRE