Synthesis of 1-(1-aroyl-2-arylvinyl)-2-dicyanome thylen-1,2-dihydropyridines from 2-chloropyridinium salts and unsaturated nitriles.

dc.contributor.author	Khoroshilov, G. E.
dc.date.accessioned	2018-03-12T10:45:13Z
dc.date.accessioned	2018-08-16T10:28:39Z
dc.date.available	2018-03-12T10:45:13Z
dc.date.available	2018-08-16T10:28:39Z
dc.date.issued	2016-01-27
dc.identifier.uri	http://dspace.ltsu.org//handle/123456789/1923
dc.description.abstract	1-(1-Aroyl-2-arylvinyl)-2-dicyanomethylene-1,2-dihydropyridines are formed from 1-(aroylmethyl)-2-chloropyridinium bromides and arylmethylenemalonitriles in ethanol at room temperature in the presence of a twofold excess of triethylamine. The products are converted into 2-amino-3-aroyl-1-cyanoindolizines on boiling in acetic acid.	ru_RU
dc.language.iso	other	ru_RU
dc.subject	1-(aroylmethyl)-2-chloropyridinium bromides, reactions with arylmethyleneindolonitriles, 1-(1-aroyl-2-arylvinyl)-2-dicyanomethylene- 1,2-dihydropyridines.	ru_RU
dc.title	Synthesis of 1-(1-aroyl-2-arylvinyl)-2-dicyanome thylen-1,2-dihydropyridines from 2-chloropyridinium salts and unsaturated nitriles.	ru_RU
dc.type	Article	ru_RU