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dc.contributor.authorYamada, Keiichien_US
dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorFujii, Sakien_US
dc.contributor.authorRavelli, Davideen_US
dc.contributor.authorFagnoni, Maurizioen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2018-08-21T05:54:14Z-
dc.date.available2018-08-21T05:54:14Z-
dc.date.issued2017-06-27en_US
dc.identifier.issn0947-6539en_US
dc.identifier.urihttp://dx.doi.org/10.1002/chem.201701865en_US
dc.identifier.urihttp://hdl.handle.net/11536/145693-
dc.description.abstractSynergistic control over the S(H)2 transition states of hydrogen abstraction exploiting polar and steric effects provides a promising cooperative strategy for site-selective C(sp(3))-H functionalization using decatungstate anion photocatalysis. By using this photocatalytic approach, the C-H bonds of substituted lactones and cyclic ketones were functionalized selectively. In the remarkable case of 2-isoamyl 4-tert-butyl cyclohexanone (1t) bearing five methyl, five methylene, and three methine C-H bonds, one methine C-H bond in the isoamyl tether was selectively functionalized.en_US
dc.language.isoen_USen_US
dc.subjectC-H functionalizationen_US
dc.subjectphotocatalysisen_US
dc.subjectsite-selectivityen_US
dc.subjectsteric effectsen_US
dc.subjectdecatungstateen_US
dc.titleCooperative Polar/Steric Strategy in Achieving Site-Selective Photocatalyzed C(sp(3))-H Functionalizationen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/chem.201701865en_US
dc.identifier.journalCHEMISTRY-A EUROPEAN JOURNALen_US
dc.citation.volume23en_US
dc.citation.spage8615en_US
dc.citation.epage8618en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000404147500012en_US
Appears in Collections:Articles