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Mendeleev Communications, 1998, Volume 8, Issue 1, Pages 23–24
DOI: https://doi.org/10.1070/MC1998v008n01ABEH000816 (Mi mendc4638) 		 
This article is cited in 19 scientific papers (total in 19 papers)

Synthesis of arylmethylenecyanothioacetamides in a Michael reaction

V. D. Dyachenkoa, S. G. Krivokolylskoa, V. P. Litvinovb

a T.G. Shevchenko Lugansk State Pedagogical Institute, Lugansk, Ukraine
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (79 kB) Citations (19)
DOI: https://doi.org/10.1070/MC1998v008n01ABEH000816
Abstract: Interaction of arylmethylenecyanoacetic esters and cyanothioacetamide in the presence of N-methylmorpholine leads to formation of arylmethylenecyanothioacetamides, which have been used in the synthesis of substituted thiazoles.
Document Type: Article
Language: English


Citation: V. D. Dyachenko, S. G. Krivokolylsko, V. P. Litvinov, “Synthesis of arylmethylenecyanothioacetamides in a Michael reaction”, Mendeleev Commun., 8:1 (1998), 23–24
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    • This publication is cited in the following 19 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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