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:

10665285

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. © 2011 Springer-Verlag.

Author keywords:

acetylenedicarboxylates; heterocyclization; malonodithioamides; thiazolidinones

Index keywords:

нет данных

DOI:

10.1007/s11172-011-0159-y

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-83455263728&doi=10.1007%2fs11172-011-0159-y&partnerID=40&md5=2c2f48e609733c5c55dda497a683af93

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Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-83455263728&doi=10.1007%2fs11172-011-0159-y&partnerID=40&md5=2c2f48e609733c5c55dda497a683af93
Affiliations	Ural Federal University, 19 ul. Mira, Ekaterinburg 620002, Russian Federation
Author Keywords	acetylenedicarboxylates; heterocyclization; malonodithioamides; thiazolidinones
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Correspondence Address	Morzherin, Yu.Yu.; Ural Federal University, 19 ul. Mira, Ekaterinburg 620002, Russian Federation; email: morzherin@mail.ustu.ru
Language of Original Document	English
Abbreviated Source Title	Russ. Chem. Bull.
Source	Scopus