Simple stepwise route to 1-substituted 2-amino-3-ethoxycarbonylindolizines.

dc.contributor.author	Khoroshilov, G. E.
dc.contributor.author	Tverdokhleb, N. M.
dc.contributor.author	Brovarets, V. S.
dc.contributor.author	Babaev, E. V.
dc.date.accessioned	2018-03-12T10:55:23Z
dc.date.accessioned	2018-08-16T10:28:31Z
dc.date.available	2018-03-12T10:55:23Z
dc.date.available	2018-08-16T10:28:31Z
dc.date.issued	2016-01-27
dc.identifier.uri	http://dspace.ltsu.org//handle/123456789/1926
dc.description.abstract	2-Chloro-N-ethoxycarbonylmethylpyridinium bromide reacts with substituted acetonitriles in two steps; the initially formed pyridine anhydro baseses undergo further ring closure to 2-amino-3-ethoxycarbon-ylindolizines.	ru_RU
dc.language.iso	other	ru_RU
dc.subject	2-Aminoindolizine Pyrrole ring synthesis CH-acids 2-Chloro-Nethoxycarbonyl-methylpyridinium bromide.	ru_RU
dc.title	Simple stepwise route to 1-substituted 2-amino-3-ethoxycarbonylindolizines.	ru_RU
dc.type	Article	ru_RU