Reactions of malonodithioamides with acetylenedicarboxylic esters

Autor:	Yu. Yu. Morzherin, Vasiliy A. Bakulev, M. F. Kosterina, Konstantin L. Obydennov, Elena L. Klimareva
Rok vydání:	2011
Předmět:	inorganic chemicals chemistry.chemical_classification Intramolecular reaction Thiazolidines chemistry.chemical_element General Chemistry Triple bond Medicinal chemistry Sulfur Adduct chemistry Nitrogen atom Group (periodic table) Organic chemistry Thioamide
Zdroj:	Russian Chemical Bulletin. 60:1016-1018
ISSN:	1573-9171 1066-5285
Popis:	Reactions of malonothioamides with acetylenedicarboxylates proceed as an addition of the sulfur atom at the triple bond with subsequent intramolecular reaction between the ester group and the nitrogen atom, that leads to substituted thiazolidines. Unsubstituted malonodithioamide and N-cyclohexylmalonodithioamide give adducts involving both thioamide fragments, whereas N,N′-bis(4-methoxyphenyl)malonodithioamide forms the 1: 1 adducts.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::626f9db584ac355396f4085c58e5876c https://doi.org/10.1007/s11172-011-0159-y Zobrazit plný text záznamu Full text from SpringerLink