New route to bioactive 2-(hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/11678

Title:	New route to bioactive 2-(hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines
Authors:	Demidov, O. P. Демидов, О. П.
Keywords:	Azepine–pyrazine recyclization;Baryl(heteroaryl)ethylamines;Bioactive amines;Fused dihydroazepines;Ring opening reactions
Issue Date:	2020
Publisher:	Elsevier Ltd
Citation:	Zubenko, A.A., Morkovnik, A.S., Divaeva, L.N., Demidov, O.P., Sochnev, V.S., Borodkina, I.G., Drobin, Y.D., Spasov, A.A. New route to bioactive 2-(hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines // Mendeleev Communications. - 2020. - Volume 30. - Issue 1. - Pages 28-30
Series/Report no.:	Mendeleev Communications
Abstract:	Nucleophilic heterocyclic ring opening in fused 7-acyl- H+ 1,2-dihydroazepines with o-phenylenediamine affords b-(hetero)arylethylamines
URI:	http://hdl.handle.net/20.500.12258/11678
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

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