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Synthesis of arylmethylenecyanothioacetamides in a Michael reaction

Vladimir Danilovich Dyachenko 1
Vladimir Danilovich Dyachenko
, 
Sergey Gennadievich Krivokolylsko 1
Sergey Gennadievich Krivokolylsko
, 
Victor Petrovich Litvinov 2
Victor Petrovich Litvinov
1 T.G. Shevchenko Lugansk State Pedagogical Institute, Lugansk, Ukraine
10.1070/MC1998v008n01ABEH000816
Published 1998-02-28
Communication , Volume 8, Issue 1, 23-24
19
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Dyachenko V. D., Krivokolylsko S. G., Litvinov V. P. Synthesis of arylmethylenecyanothioacetamides in a Michael reaction // Mendeleev Communications. 1998. Vol. 8. No. 1. pp. 23-24.
GOST all authors (up to 50) Copy
Dyachenko V. D., Krivokolylsko S. G., Litvinov V. P. Synthesis of arylmethylenecyanothioacetamides in a Michael reaction // Mendeleev Communications. 1998. Vol. 8. No. 1. pp. 23-24.
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TY - JOUR
DO - 10.1070/MC1998v008n01ABEH000816
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n01ABEH000816
TI - Synthesis of arylmethylenecyanothioacetamides in a Michael reaction
T2 - Mendeleev Communications
AU - Dyachenko, Vladimir Danilovich
AU - Krivokolylsko, Sergey Gennadievich
AU - Litvinov, Victor Petrovich
PY - 1998
DA - 1998/02/28
PB - Mendeleev Communications
SP - 23-24
IS - 1
VL - 8
ER -
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@article{1998_Dyachenko,
author = {Vladimir Danilovich Dyachenko and Sergey Gennadievich Krivokolylsko and Victor Petrovich Litvinov},
title = {Synthesis of arylmethylenecyanothioacetamides in a Michael reaction},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n01ABEH000816},
number = {1},
pages = {23--24},
doi = {10.1070/MC1998v008n01ABEH000816}
}
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Dyachenko, Vladimir Danilovich, et al. “Synthesis of arylmethylenecyanothioacetamides in a Michael reaction.” Mendeleev Communications, vol. 8, no. 1, Feb. 1998, pp. 23-24. https://mendcomm.colab.ws/publications/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.

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