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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18095
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dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.date.accessioned2021-09-06T13:33:42Z-
dc.date.available2021-09-06T13:33:42Z-
dc.date.issued2021-
dc.identifier.citationZubenko, A. A.; Sochnev, V. S.; Kartsev, V. G.; Divaeva L. N.; Demidov, O. P.; Klimenko A. I.; Bodryakov A. N.; Bodryakova M. A.; Borodkin, G. S.; Morkovnik, A. S. Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion // Mendeleev Communications. - 2021. - Том 31. - Выпуск 4. - Стр.: 545 - 547ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18095-
dc.description.abstractNew 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 ringru
dc.language.isoenru
dc.publisherElsevier Ltdru
dc.relation.ispartofseriesMendeleev Communications-
dc.subjectRecyclizationru
dc.subjectAzepino[4; benzo[d ]azepinesru
dc.subject5-b]indolesru
dc.subjectAzepinonesru
dc.subjectBetainesru
dc.subjectDithiocarboxylatesru
dc.subjectIminium saltsru
dc.subjectIsoquinolinium saltsru
dc.subjectThioamidesru
dc.titleSystems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansionru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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