Synthesis of Novel Triazolyl-substituted Carboxylic Acid Esters and Their Aminolysis

Autor:	Leonid D. Popov, N. I. Vikrishchuk
Rok vydání:	2019
Předmět:	chemistry.chemical_compound Aminolysis 010405 organic chemistry Chemistry Organic Chemistry Organic chemistry Substituted carboxylic acid Alkylation Ethyl chloroacetate 01 natural sciences 0104 chemical sciences
Zdroj:	Russian Journal of Organic Chemistry. 55:234-240
ISSN:	1608-3393 1070-4280
DOI:	10.1134/s1070428019020155
Popis:	Recyclization of 4-oxo-1,3-benzoxazinium perchlorates under the action of hydrazinobenzoic acids gave previously unknown 1,2,4-triazolylbenzoic acids which were esterified to obtain the corresponding esters. Alkylation of 3-(o-hydroxyphenyl)-1,2,4-triazoles with ethyl chloroacetate formed ethyl triazolylacetates, whose aminolysis allowed synthesis of novel bis-heterocyclic imides.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::b8a2c56b879af84d0a675df65f76dd45 https://doi.org/10.1134/s1070428019020155 Zobrazit plný text záznamu Plný text ve formátu PDF