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Please use this identifier to cite or link to this item: http://lib.hpu.edu.vn/handle/123456789/21905
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dc.contributor.authorArimori, Sadayukien_US
dc.contributor.authorMatsubara, Okiyaen_US
dc.contributor.authorTakada, Masahiroen_US
dc.date.accessioned2016-07-04T03:49:04Z
dc.date.available2016-07-04T03:49:04Z
dc.date.issued2016en_US
dc.identifier.otherHPU4160388en_US
dc.identifier.urihttps://lib.hpu.edu.vn/handle/123456789/21905-
dc.description.abstractDifluoromethanesulfonyl hypervalent iodonium ylides 2 were developed as electrophilic difluoromethylthiolation reagents for a wide range of nucleophiles. Enamines, indoles, β-keto esters, silyl enol ethers and pyrroles were effectively reacted with2affording desired difluoromethylthio (SCF2H)-substituted compounds in good to high yields under copper catalysis.en_US
dc.format.extent9 p.en_US
dc.format.mimetypeapplication/pdf-
dc.language.isoenen_US
dc.subjectOrganic chemistryen_US
dc.subjectSyntheticen_US
dc.subjectChemistryen_US
dc.subjectOrganometallic chemistryen_US
dc.subjectDifluoromethylthiolationen_US
dc.subjectHypervalenten_US
dc.subjectIodoniumylideen_US
dc.subjectCarbeneen_US
dc.subjectSulfuren_US
dc.subjectFluorineen_US
dc.titleDifluoromethanesulfonyl hypervalent iodoniumylides for electrophilic difluoromethylthiolation reactions under copper catalysisen_US
dc.typeArticleen_US
dc.size764KBen_US
dc.departmentEducationen_US
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