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JOURNALS
// Mendeleev Communications
// Archive
Mendeleev Commun.,
1998
Volume 8,
Issue 1,
Pages
23–24
(Mi mendc4638)
This article is cited in
21
papers
Synthesis of arylmethylenecyanothioacetamides in a Michael reaction
V. D. Dyachenko
a
,
S. G. Krivokolylsko
a
,
V. P. Litvinov
b
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
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.
Language:
English
DOI:
10.1070/MC1998v008n01ABEH000816
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