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JOURNALS // Mendeleev Communications // Archive

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. Sochneva, A. S. Morkovnika, A. A. Zubenkob, L. N. Divaevaa, O. P. Demidovc, T. N. Gribanovaa, L. N. Fetisovb, V. V. Chekryshevab, K. N. Kononenkob, M. A. Bodryakovab, A. I. Klimenkob, G. S. Borodkina, I. A. Estrind

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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