Unexpected Formation of 6,7-Dihydrobenzo[4',5']imidazo-[1 ',2': 1,6]pyrimido[5,4-a]indolizine Derivative in the Alkylation of 2-Amino-1-(benzimidazol-2-yl)-3-(4-methoxybenzoyl)indolizine.

dc.contributor.author	Saraeva, T. A.
dc.contributor.author	Khoroshilov, G. E.
dc.contributor.author	Brovarets, V. S.
dc.contributor.author	Zubatyuk, R. I.
dc.contributor.author	Shishkin, O. V.
dc.date.accessioned	2018-03-12T10:47:44Z
dc.date.accessioned	2018-08-16T10:28:34Z
dc.date.available	2018-03-12T10:47:44Z
dc.date.available	2018-08-16T10:28:34Z
dc.date.issued	2016-01-27
dc.identifier.uri	http://dspace.ltsu.org//handle/123456789/1924
dc.description.abstract	An attempt to effect exhaustive alkylation of 2-amino-1-(benzimidazol-2-yl)-3-(4-methoxybenzoyl) indolizine with alkyl iodides in boiling acetone led to the formation of 6,6-dimethyl-8-(4-methoxybenzoyl)-6,7-dihydrobenzo[4',5']imidazo[1',2' : 1,6]pyrimido[5,4-a]indolizine instead of expected N-alkyl derivatives. The product structure was proved by X-ray analysis.	ru_RU
dc.language.iso	other	ru_RU
dc.title	Unexpected Formation of 6,7-Dihydrobenzo[4',5']imidazo-[1 ',2': 1,6]pyrimido[5,4-a]indolizine Derivative in the Alkylation of 2-Amino-1-(benzimidazol-2-yl)-3-(4-methoxybenzoyl)indolizine.	ru_RU
dc.type	Article	ru_RU