Chemistry of Heterocyclic Compounds p. 77 - 83 (1985)
Update date:2022-08-02
Topics:
Krauze, A. A.
Liepin'sh, E. E.
Pelcher, Yu. E.
Kalme, Z. A.
Dipan, I. V.
Dubur, G. Ya.
The condensation of ethyl arylideneacetoacetate with cyanothioacetamide and of arylidenecyanothioacetamides with ethyl acetoacetate or of arylidenecyanothioacetamides with ethyl β-aminocrotonate gave 3-cyano-4-aryl-5-ethoxycarbonyl-6-methyl-3,4-dihydropyridine-2-thiones.PMR spectroscopy showed that the 3-cyano-4-aryl-3,4-dihydropyridine-2-thiones are formed as a mixture of cis and trans isomers.
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Doi:10.1021/jo00221a004
(1985)Doi:10.1016/S0040-4020(01)96415-4
(1985)Doi:10.1021/jm00117a014
(1988)Doi:10.1021/jm00149a015
(1985)Doi:10.1016/S0040-4020(01)86394-8
(1991)Doi:10.1007/BF00515081
(1985)
