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dc.contributor.authorOwston, Nathan A.
dc.contributor.authorFu, Gregory C.
dc.date.accessioned2013-11-15T14:21:40Z
dc.date.available2013-11-15T14:21:40Z
dc.date.issued2010-09
dc.date.submitted2010-07
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/82112
dc.description.abstractA method for asymmetric alkyl−alkyl Suzuki reactions of unactivated secondary alkyl electrophiles, specifically, cross-couplings of racemic acylated halohydrins with alkylborane reagents, has been developed. A range of protected bromohydrins, as well as a protected chlorohydrin and a homologated bromohydrin, are coupled in good ee by a catalyst derived from commercially available components.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (National Institute of General Medical Sciences, Grant R01- GM62871)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ja105924fen_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.sourcePMCen_US
dc.titleAsymmetric Alkyl−Alkyl Cross-Couplings of Unactivated Secondary Alkyl Electrophiles: Stereoconvergent Suzuki Reactions of Racemic Acylated Halohydrinsen_US
dc.typeArticleen_US
dc.identifier.citationOwston, Nathan A., and Gregory C. Fu. “Asymmetric Alkyl−Alkyl Cross-Couplings of Unactivated Secondary Alkyl Electrophiles: Stereoconvergent Suzuki Reactions of Racemic Acylated Halohydrins.” Journal of the American Chemical Society 132, no. 34 (September 2010): 11908-11909.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorOwston, Nathan A.en_US
dc.contributor.mitauthorFu, Gregory C.en_US
dc.relation.journalJournal of the American Chemical Societyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsOwston, Nathan A.; Fu, Gregory C.en_US
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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