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dc.contributor.authorUno, Misaeen_US
dc.contributor.authorSumino, Shuheien_US
dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorMatsuura, Makotoen_US
dc.contributor.authorKuroki, Yoshichikaen_US
dc.contributor.authorKishikawa, Yosukeen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2019-09-02T07:46:16Z-
dc.date.available2019-09-02T07:46:16Z-
dc.date.issued2019-07-19en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.joc.9b00901en_US
dc.identifier.urihttp://hdl.handle.net/11536/152661-
dc.description.abstractPhotoredox-catalyzed allylation of alpha-gem-difluorinated organohalides with allyl sulfones proceeded smoothly under visible light irradiation to give 4,4-difluoroalkenes in good yields. In the presence of catalytic Ru(bpy)(3)Cl-2, Hantzsch ester, and diisopropylethylamine, the reaction was complete within 2 h. Using the same methodology, three-component cascade reactions to give 6,6-difluoroalkenes were carried out successfully.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of 4,4-Difluoroalkenes by Coupling of alpha-Substituted alpha,alpha-Difluoromethyl Halides with Allyl Sulfones under Photoredox Catalyzed Conditionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.joc.9b00901en_US
dc.identifier.journalJOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volume84en_US
dc.citation.issue14en_US
dc.citation.spage9330en_US
dc.citation.epage9338en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000476957000047en_US
dc.citation.woscount0en_US
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