Sciact
  • EN
  • RU

Reactions of N,N-(dialkyl)arylthioacetamides with dialkyl acetylenedicarboxylates Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2002, Volume: 51, Number: 4, Pages: 613-618 Pages count : 6 DOI: 10.1023/A:1015868201847
Tags Condensation; Dialkyl acetylenedicarboxylates; N,N-(dialkyl)arylthioacetamides; Thiophene
Authors Kosterina M.F. 1 , Morzherin Yu.Yu. 1 , Tkachev A.V. 2 , Rybalova T.V. 2 , Gatilov Yu.V. 2 , Bakulev V.A. 1
Affiliations
1 (Scopus) Ural State Technical University, 19 ul. Mira, 620002 Yekaterinburg, Russian Federation
2 (Scopus) N. N. Vorozhtsov Novosibirsk I., Siberian Br. Russ. Acad. of Sci., 9 prosp. Akad. Lavrent'eva, 630090 Novosibirsk, Russian Federation

Abstract: 2-(Alkoxycarbonylmethylidene)-4-aryl-5-(dialkylamino)thiophen-3(2H)-ones were synthesized by condensation of N,N-(dialkyl)arylthioacetamides with dialkyl acetylene-dicarboxylates. Intermediate substituted vinylic sulfides were isolated. When heated or in the presence of an acid or a base, they undergo cyclization into thiophenes.
Cite: Kosterina M.F. , Morzherin Y.Y. , Tkachev A.V. , Rybalova T.V. , Gatilov Y.V. , Bakulev V.A.
Reactions of N,N-(dialkyl)arylthioacetamides with dialkyl acetylenedicarboxylates
Russian Chemical Bulletin. 2002. V.51. N4. P.613-618. DOI: 10.1023/A:1015868201847 WOS Scopus РИНЦ OpenAlex
Identifiers:
Web of science: WOS:000176530300014
Scopus: 2-s2.0-0141609831
Elibrary: 13416472
OpenAlex: W2951598076
Citing:
DB Citing
Scopus 1
Web of science 14
Elibrary 10
OpenAlex 15
Altmetrics: