A. A. Zubenko, V. S. Sochnev, V. G. Kartsev, L. N. Divaeva, O. P. Demidov, A. I. Klimenko, A. N. Bodryakov, M. A. Bodryakova, G. S. Borodkin, A. S. Morkovnik, “Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion”, Mendeleev Commun., 2021, Volume 31, Issue 4,Pages <nobr>545

This article is cited in 2 papers

Communications

Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion

A. A. Zubenko^a, V. S. Sochnev^b, V. G. Kartsev^c, L. N. Divaeva^b, O. P. Demidov^d, A. I. Klimenko^a, A. N. Bodryakov^a, M. A. Bodryakova^a, G. S. Borodkin^b, A. S. Morkovnik^b

^a North-Caucasian Zonal Research Veterinary Institute, Novocherkassk, Russian Federation
^b Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
^c 'InterBioScreen Ltd.', Chernogolovka, Moscow Region, Russian Federation
^d North-Caucasus Federal University, Stavropol, Russian Federation

Abstract: New 1-oxo-2-thioxo-1,2,4,5-tetrahydrobenz[d]azepine and 1-oxo-2-thioxo-1,2,4,5-tetrahydroazepino[4,5-b]indole derivatives were conveniently obtained by the novel recyclization reaction of (methylthio)carbonothioylsubstituted heterocyclic quaternary salts with expansion of the dihydropyridine ring.

Language: English

DOI: 10.1016/j.mencom.2021.07.036

	*Supplementary materials:*
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