Mendeleev Commun., 2022 Volume 32, Issue 6, Pages 795–797
(Mi mendc802)
This article is cited in
3 papers
Communications
Novel recyclization of 3,4-dihydroisoquinolines as an efficient route to a new type of heteroarylated derivatives of β-arylethylamines
V. S. Sochnev a ,
A. S. Morkovnik a ,
A. A. Zubenko b ,
L. N. Divaeva a ,
O. P. Demidov c ,
T. N. Gribanova a ,
L. N. Fetisov b ,
V. V. Chekrysheva b ,
K. N. Kononenko b ,
M. A. Bodryakova b ,
A. I. Klimenko b ,
G. S. Borodkin a ,
I. A. Estrin d a Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
b North-Caucasian Zonal Research Veterinary Institute, Novocherkassk, Russian Federation
c North-Caucasus Federal University, Stavropol, Russian Federation
d Rostov State Transport University, Rostov-on-Don, Russian Federation
Abstract:
A new recyclization of 3,4-dihydroisoquinolines is a convenient route to derivatives of new bbb-(o-benzothienylaryl)-and bbb-(o-thieno[2,3-b]pyridinylaryl)-containing ethylamines. These compounds look promising monoaminergic agents.
Keywords:
3,4-dihydroisoquinolines, β-arylethylamines, recyclization, heterocyclization, o -benzothienylarenes, o -thieno[2,3-b ]pyridinyl- arenes.
Language: English
DOI:
10.1016/j.mencom.2022.11.029
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