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dc.contributor.authorGribble, Michael William
dc.contributor.authorPirnot, Michael T
dc.contributor.authorBandar, Jeffrey
dc.contributor.authorLiu, Richard
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2018-01-10T15:41:53Z
dc.date.available2018-01-10T15:41:53Z
dc.date.issued2017-01
dc.date.submitted2016-12
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/113039
dc.description.abstractWe report a highly enantioselective CuH-catalyzed Markovnikov hydrosilylation of vinylarenes and vinyl heterocycles. This method has a broad scope and enables both the synthesis of isolable silanes and the conversion of crude products to chiral alcohols. Density functional theory calculations support a mechanism proceeding by hydrocupration followed by σ-bond metathesis with a hydrosilane.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Award GM46059)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Postdoctoral Fellowship 1F32GM113311)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Postdoctoral Fellowship GM112197)en_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/JACS.6B13029en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceACSen_US
dc.titleAsymmetric Copper Hydride-Catalyzed Markovnikov Hydrosilylation of Vinylarenes and Vinyl Heterocyclesen_US
dc.typeArticleen_US
dc.identifier.citationGribble, Michael W., et al. “Asymmetric Copper Hydride-Catalyzed Markovnikov Hydrosilylation of Vinylarenes and Vinyl Heterocycles.” Journal of the American Chemical Society, vol. 139, no. 6, Feb. 2017, pp. 2192–95. © 2017 American Chemical Society.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorGribble, Michael William
dc.contributor.mitauthorPirnot, Michael T
dc.contributor.mitauthorBandar, Jeffrey
dc.contributor.mitauthorLiu, Richard
dc.contributor.mitauthorBuchwald, Stephen Leffler
dc.relation.journalJournal of the American Chemical Societyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-01-09T18:43:28Z
dspace.orderedauthorsGribble, Michael W.; Pirnot, Michael T.; Bandar, Jeffrey S.; Liu, Richard Y.; Buchwald, Stephen L.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2008-3264
dc.identifier.orcidhttps://orcid.org/0000-0002-7896-1683
dc.identifier.orcidhttps://orcid.org/0000-0001-5418-3082
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licensePUBLISHER_POLICYen_US


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