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dc.contributor.authorOsborne, Hugh C
dc.contributor.authorDurie, A.
dc.contributor.authorSchmidt, Christine K
dc.contributor.authorLarrosa, I.
dc.date.accessioned2020-12-08T05:36:35Z
dc.date.available2020-12-08T05:36:35Z
dc.date.issued2020en
dc.identifier.citationOsborne HC, Durie A, Schmidt CK, Larrosa I. C–H Borylation: No Need to Stop for Directions. Trends in Chemistry. 2020;2(11):957-9.en
dc.identifier.doi10.1016/j.trechm.2020.07.009en
dc.identifier.urihttp://hdl.handle.net/10541/623515
dc.description.abstractA recent work by Hartwig et al. details an efficient method to borylate strong primary C(sp3)–H bonds via iridium-catalysed C–H activation. The conditions confer counterintuitive selectivity over more labile C–H bonds, while providing an avenue for a gamut of synthetically valuable late-stage functionalisations through versatile borylate intermediates.en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1016/j.trechm.2020.07.009en
dc.titleC-H Borylation: no need to stop for directionsen
dc.typeArticleen
dc.contributor.departmentDepartment of Chemistry, School of Natural Sciences, University of Manchester, Oxford Road, Manchester M13 9PL,en
dc.identifier.journalTrends in Chemistryen
dc.description.noteen]


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