Reaction of (p-alkoxyphenyl)-acetothioamides with acetylene-dicarboxylic esters

Autor:	Yu. V. Gatilov, M. F. Kosterina, Yu. Yu. Morzherin, Tatyana V. Rybalova
Rok vydání:	2009
Předmět:	chemistry.chemical_compound Acetylene chemistry Intramolecular force Organic Chemistry Condensation Alkoxy group Thiophene Organic chemistry Medicinal chemistry
Zdroj:	Chemistry of Heterocyclic Compounds. 45:422-425
ISSN:	1573-8353 0009-3122
Popis:	The condensation of p-methoxy(ethoxy)phenylacetothioamides with acetylenedicarboxylic esters leads to two condensation products, 2-(alkoxycarbonylmethylene)-4-(4-methoxy(ethoxy)phenyl)-5-morpho-lino-3H-thiophen-3-ones and 2-(alkoxycarbonylmethylene)-4-(4-methoxy(ethoxy)phenyl)-5-alkoxy-3H-thiophen-3-ones. It was shown that the substitution of the morpholino group is intramolecular.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::72c4a9954830ffc5c1967fe21021259b https://doi.org/10.1007/s10593-009-0291-x Zobrazit plný text záznamu Plný text ve formátu PDF