Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/9753
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dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2019-12-19T14:06:08Z-
dc.date.available2019-12-19T14:06:08Z-
dc.date.issued2019-
dc.identifier.citationGateev, AR; Dmitriev, MV; Mokrushin, IG; Mashevskaya, IV; Mastivets, AN; Rubin, M. Synthesis of meta-substituted anilines via a three-component reaction of acetone, amines, and 1,3-diketones // ORGANIC & BIOMOLECULAR CHEMISTRY. - 2019. - Том: 17. - Выпуск: 47. - Стр.: 10030-10044ru
dc.identifier.urihttp://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=1&SID=C2RI3BOJAwOaexjHfEf&page=1&doc=1-
dc.identifier.urihttp://hdl.handle.net/20.500.12258/9753-
dc.description.abstractA facile method for the synthesis of meta-substituted arylamines from acyclic precursors was developed. This method is based on three-component cyclo-condensation/aromatization of in situ generated imines of acetone with 1,3-diketones either under conventional heating or under microwave irradiation. The utility of this methodology is illustrated by the possibility of a gram scale synthesis of various anilines from readily available reagentsru
dc.language.isoenru
dc.publisherROYAL SOC CHEMISTRYru
dc.relation.ispartofseriesOrganic and Biomolecular Chemistry-
dc.subjectPd-at-paniru
dc.subjectPharmacokinetic propertiesru
dc.subjectTrifluoromethyl ketonesru
dc.subjectPactical catalystru
dc.subjectDiscoveryru
dc.subjectInhibitorsru
dc.subjectPotentru
dc.subjectBenzannulationru
dc.subjectCondensationru
dc.subjectBicalutamideru
dc.titleSynthesis of meta-substituted anilines via a three-component reaction of acetone, amines, and 1,3-diketonesru
dc.typeСтатьяru
vkr.amountСтр.: 10030-10044ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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