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dc.contributor.authorCartier, Alexen_US
dc.contributor.authorLevernier, Etienneen_US
dc.contributor.authorCorce, Vincenten_US
dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorDhimane, Anne-Liseen_US
dc.contributor.authorOllivier, Cyrilen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.contributor.authorFensterbank, Louisen_US
dc.date.accessioned2019-04-02T05:58:10Z-
dc.date.available2019-04-02T05:58:10Z-
dc.date.issued2019-02-04en_US
dc.identifier.issn1433-7851en_US
dc.identifier.urihttp://dx.doi.org/10.1002/anie.201811858en_US
dc.identifier.urihttp://hdl.handle.net/11536/148882-
dc.description.abstractPrimary, secondary, and tertiary alkyl radicals formed by the photocatalyzed oxidation of organosilicates underwent efficient carbonylation with carbon monoxide (CO) to give a variety of unsymmetrical ketones. This study introduces the possibility of radical carbonylation under a photooxidative regime.en_US
dc.language.isoen_USen_US
dc.subjectcarbonylationen_US
dc.subjectphotocatalysisen_US
dc.subjectradicalsen_US
dc.subjectsilicatesen_US
dc.subjectthree-component reactionsen_US
dc.titleCarbonylation of Alkyl Radicals Derived from Organosilicates through Visible-Light Photoredox Catalysisen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/anie.201811858en_US
dc.identifier.journalANGEWANDTE CHEMIE-INTERNATIONAL EDITIONen_US
dc.citation.volume58en_US
dc.citation.spage1789en_US
dc.citation.epage1793en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000458826800043en_US
dc.citation.woscount1en_US
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