Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/9753
Title: Synthesis of meta-substituted anilines via a three-component reaction of acetone, amines, and 1,3-diketones
Authors: Rubin, M. A.
Рубин, М. А.
Keywords: Pd-at-pani;Pharmacokinetic properties;Trifluoromethyl ketones;Pactical catalyst;Discovery;Inhibitors;Potent;Benzannulation;Condensation;Bicalutamide
Issue Date: 2019
Publisher: ROYAL SOC CHEMISTRY
Citation: Gateev, 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.: 10030-10044
Series/Report no.: Organic and Biomolecular Chemistry
Abstract: A 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 reagents
URI: http://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=1&SID=C2RI3BOJAwOaexjHfEf&page=1&doc=1
http://hdl.handle.net/20.500.12258/9753
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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