Amide and thioamide of cyanoacetic acid in АdNE type reactions with 2-halopyridinium salts

dc.contributor.author	Tverdokhleb, N. M.
dc.contributor.author	Khoroshilov, G. E.
dc.date.accessioned	2019-03-09T13:16:52Z
dc.date.available	2019-03-09T13:16:52Z
dc.date.issued	2015
dc.identifier.uri	http://hdl.handle.net/123456789/3565
dc.description	Tverdokhleb N. M. Amide and thioamide of cyanoacetic acid in АdNE type reactions with 2-halopyridinium salts / N. M. Tverdokhleb, G. E. Khoroshilov // Химия гетероциклических соединений. – 2015. – №1. – С. 56–59	uk_UA
dc.description.abstract	A mixture of pyridine-2-thiones and 2-amino-1-cyanoindolizines was obtained by condensation of N-[(alkoxycarbonyl)methyl]- or N-[(aroyl)methyl]-2-chloro(bromo)pyridinium halides in the presence of 2 equivalents of triethylamine. Furthermore, reacting cyanoacetamide with N-[(alkoxycarbonyl)methyl]-2-chloro(bromo)pyridinium salts afforded a mixture of 2-amino-1-carbamoylindolizine-3-carboxylates and a novel heterocyclic system, 2,4-dioxo-2,3,4,5-tetrahydropyrido[1,2-d][1,4]diazepine-1-carbonitrile.	uk_UA
dc.language.iso	other	uk_UA
dc.subject	хімічні науки	uk_UA
dc.title	Amide and thioamide of cyanoacetic acid in АdNE type reactions with 2-halopyridinium salts	uk_UA
dc.type	Article	uk_UA