Synthesis, study of configuration and reactivity of amino acids, acylated by p-[DI-(2-chloroalkyl)amino]cinnamic acid

Autor:	L. Ya. Gurvichene, G. I. Prasmitskene, O. V. Kil'disheva, A. M. Yuodvirshis, K. I. Karpavichyus
Rok vydání:	1973
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Hydrolysis chemistry Organic chemistry Reactivity (chemistry) General Chemistry Ethyl ester Cinnamic acid Amino acid
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 22:2012-2016
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf00929394
Popis:	1. The following compounds were synthesized; p-[di-(2-chloropropyl)amino]cinnamoyl-DL-phenyl-alanine and its ethyl ester, p-[di-(2-chloropropyl)amino]cinnamoyl-DL-valine, the methyl ester of p-[di-(2-chloropropyl) amino]cinnamoyl-L-histidine, p-[di-(2-chloropropyl)amino]cinnamoyl-p-aminobenzoic acid and its ethyl ester, and also p-[di-(2-chloroethyl)amino]cinnamoyl-p-aminobenzoic acid and its ethyl ester. 2. The hydrolysis rate of the C-Cl bond in the cytotoxic groups of the synthesized compounds was measured.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::54b1d3fb0a52c792ab37c5b135874bdd https://doi.org/10.1007/bf00929394 Zobrazit plný text záznamu Full text from SpringerLink