New Example of Acyl Cleavage of Benzoyl-1,1,1-trifluoroacetone in a Three-Component Synthesis of 4-Aryl-2-thioxo-6-phenyl-1,2- dihydropyridine-3-carbonitriles.

dc.contributor.author	Dyachenko, V. D.
dc.date.accessioned	2018-03-06T06:29:22Z
dc.date.accessioned	2018-08-16T10:31:13Z
dc.date.available	2018-03-06T06:29:22Z
dc.date.available	2018-08-16T10:31:13Z
dc.date.issued	2013-10-07
dc.identifier.uri	http://dspace.ltsu.org//handle/123456789/1636
dc.description.abstract	A three-component condensation of aromatic aldehydes, cyanothioacetamide, and benzoyl-1,1,1-trifluoroacetone, involving the acyl cleavage of the latter, results in 4-aryl-2-thioxo-6-phenyl-1,2-dihydropyridine- 3-carbonitriles. Their alkylation was studied.	ru_RU
dc.language.iso	other	ru_RU
dc.title	New Example of Acyl Cleavage of Benzoyl-1,1,1-trifluoroacetone in a Three-Component Synthesis of 4-Aryl-2-thioxo-6-phenyl-1,2- dihydropyridine-3-carbonitriles.	ru_RU
dc.type	Article	ru_RU