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dc.creatorKhalafy, Jabbar
dc.creatorBadparvar, Fahimeh
dc.creatorMarjani, Ahmad Poursattar
dc.date2016-09-10
dc.date.accessioned2019-11-13T15:11:23Z
dc.date.available2019-11-13T15:11:23Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/89
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/112523
dc.descriptionAn efficient method for the synthesis of 1-aryl-6,6-dimethyl-2-phenyl-6,7-dihydro-1H-indol-4(5H)-ones is achieved in two steps, using a three-component reaction of phenacyl bromide, dimedone and aniline derivatives in water-ethanol (1:1) under reflux conditions. en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/89/75
dc.rightsCopyright (c) 2017 Jabbar Khalafy, Fahimeh Badparvar, Ahmad Poursattar Marjanien-US
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 61 No 3 (2016): Journal of the Chilean Chemical Societyen-US
dc.source0717-9707
dc.source0717-9324
dc.subjectPhenacyl bromideen-US
dc.subjectDimedoneen-US
dc.subjectAnilinesen-US
dc.subject1H-Indol-4(5H)-onesen-US
dc.subjectThree-component reactionen-US
dc.titleSYNTHESIS OF 1-ARYL-6,6-DIMETHYL-2-PHENYL-6,7-DIHYDRO-1H-INDOL-4(5H)-ONES BY TWO STEPS, IN A THREE-COMPONENT REACTIONen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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