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

[Display omitted] Nucleophilic heterocyclic ring opening in fused 7-acyl- H+ 1,2-dihydroazepines with o-phenylenediamine affords b-(hetero)arylethylamines.

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Bibliographic Details
Published in:Mendeleev communications 2020-01, Vol.30 (1), p.28-30
Main Authors: Zubenko, Alexander A., Morkovnik, Anatolii S., Divaeva, Lyudmila N., Demidov, Oleg P., Sochnev, Vadim S., Borodkina, Inna G., Drobin, Yuriy D., Spasov, Alexander A.
Format: Article
Language:English
Subjects:
azepine–pyrazine recyclization
baryl(heteroaryl)ethylamines
bioactive amines
fused dihydroazepines
ring opening reactions
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Description
Summary:[Display omitted] Nucleophilic heterocyclic ring opening in fused 7-acyl- H+ 1,2-dihydroazepines with o-phenylenediamine affords b-(hetero)arylethylamines.
ISSN:0959-9436
DOI:10.1016/j.mencom.2020.01.009