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dc.contributor.author이상기*
dc.contributor.authorJean Bouffard*
dc.date.accessioned2017-10-27T11:45:23Z-
dc.date.available2017-10-27T11:45:23Z-
dc.date.issued2017*
dc.identifier.issn0306-0012*
dc.identifier.otherOAK-21026*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/237191-
dc.description.abstractRecent advances in transition metal-catalyzed C-H bond functionalization have profoundly impacted synthetic strategy. Since organic substrates typically contain several chemically distinct C-H bonds, controlling the regioselectivity of C-H bond functionalization is imperative to harness its full potential. Moreover, the ability to alter reaction pathways to selectively functionalize different C-H bonds in a substrate represents a greater opportunity and challenge. The choice of catalysts, ligands, solvents, and even more subtle variations of the reaction conditions have been shown to allow the formation of regioisomeric C-H functionalization products starting from the same precursors. This review describes recent advances in transition metal-catalyzed divergent C-H bond functionalization that highlight its potential in organic synthesis. © 2017 The Royal Society of Chemistry.*
dc.languageEnglish*
dc.publisherRoyal Society of Chemistry*
dc.titleTransition metal-catalyzed site- and regio-divergent C-H bond functionalization*
dc.typeReview*
dc.relation.issue14*
dc.relation.volume46*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage4299*
dc.relation.lastpage4328*
dc.relation.journaltitleChemical Society Reviews*
dc.identifier.doi10.1039/c7cs00064b*
dc.identifier.wosidWOS:000405683200008*
dc.identifier.scopusid2-s2.0-85024905664*
dc.author.googlePing L.*
dc.author.googleChung D.S.*
dc.author.googleBouffard J.*
dc.author.googleLee S.-G.*
dc.contributor.scopusid이상기(15082786300)*
dc.contributor.scopusidJean Bouffard(8892273200)*
dc.date.modifydate20240123104103*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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