Peptide modification by incorporation of α-trifluoromethyl α-amino acids via trifluoromethyl-substituted acylimines

Autor:	Klaus Burger, Martin Rudolph, E. Höss, L. Seymour, Christian Schierlinger
Rok vydání:	1993
Předmět:	chemistry.chemical_classification Peptide modification Dipeptide Trifluoromethyl Stereochemistry Organic Chemistry Quinoline Liquid phase Biochemistry Amino acid Inorganic Chemistry chemistry.chemical_compound chemistry Peptide synthesis Environmental Chemistry Physical and Theoretical Chemistry
Zdroj:	Journal of Fluorine Chemistry. 61:163-170
ISSN:	0022-1139
DOI:	10.1016/s0022-1139(00)80427-3
Popis:	α-Trifluoromethyl-substituted α-amino acids can be introduced into the C-terminal position of peptides via acylimines obtained on reaction of trifluoropyruvates with N-protected α-amino acid amides and dipeptide amides, respectively.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::25fa250c99b49f0c5243fddd154f1776 https://doi.org/10.1016/s0022-1139(00)80427-3 Zobrazit plný text záznamu