Reactions of malonodithioamides with acetylenedicarboxylic esters / Obydennov K. L.,Kosterina M. F.,Klimareva E. L.,Bakulev V. A.,Morzherin Yu. Yu. // RUSSIAN CHEMICAL BULLETIN. - 2011. - V. 60, l. 5. - P. 1016-1018.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

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.

Author keywords:

thiazolidinones; malonodithioamides; acetylenedicarboxylates; heterocyclization DITHIOMALONIC ACID DIANILIDE; THIAZOLIDIN-4-ONES; KETONES

DOI:

нет данных

Web of Science ID:

ISI:000297153800035

Соавторы в МНС:

Другие поля

Поле	Значение
Month	MAY
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	DITHIOMALONIC ACID DIANILIDE; THIAZOLIDIN-4-ONES; KETONES
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	morzherin@mail.ustu.ru
ResearcherID-Numbers	Morzherin, Yury/M-7420-2013 Obydennov, Konstantin/M-7550-2013
ORCID-Numbers	Morzherin, Yury/0000-0002-1333-6676 Obydennov, Konstantin/0000-0002-5884-4105
Number-of-Cited-References	14
Usage-Count-Last-180-days	3
Usage-Count-Since-2013	22
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	849VQ