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dc.contributor.authorUeda, Mitsuhiroen_US
dc.contributor.authorMaeda, Ayamien_US
dc.contributor.authorHamaoka, Kanakoen_US
dc.contributor.authorSasano, Mikaen_US
dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2019-04-02T05:58:20Z-
dc.date.available2019-04-02T05:58:20Z-
dc.date.issued2019-03-01en_US
dc.identifier.issn0039-7881en_US
dc.identifier.urihttp://dx.doi.org/10.1055/s-0037-1610413en_US
dc.identifier.urihttp://hdl.handle.net/11536/148939-
dc.description.abstractThe C(sp(3))-H allylation of alkanes is investigated by using allyl bromides under radical reaction conditions. In many cases, methine C-H allylation preceded methylene and methyl C-H allylation with complete or a high degree of site selectivity. The C-H allylation of allylic compounds, such as allylbenzene, gives 1,5-dienes with the S(H)2' reactions of the allyl radicals occurring at the less hindered carbon.en_US
dc.language.isoen_USen_US
dc.subjectC(sp(3))-H allylationen_US
dc.subjectbromine radicalsen_US
dc.subjectS(H)2 reactionen_US
dc.subjectS(H)2 ' reactionen_US
dc.subjectsite selectivityen_US
dc.titleBromine-Radical-Mediated Site-Selective Allylation of C(sp(3))-H Bondsen_US
dc.typeArticleen_US
dc.identifier.doi10.1055/s-0037-1610413en_US
dc.identifier.journalSYNTHESIS-STUTTGARTen_US
dc.citation.volume51en_US
dc.citation.spage1171en_US
dc.citation.epage1177en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000459926800015en_US
dc.citation.woscount0en_US
Appears in Collections:Articles