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dc.contributor.authorLou, Sha
dc.contributor.authorFu, Gregory C.
dc.date.accessioned2011-09-21T19:09:09Z
dc.date.available2011-09-21T19:09:09Z
dc.date.issued2010-03
dc.date.submitted2010-02
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/65912
dc.description.abstractA new family of organometallic compounds, organozirconium reagents, are shown to serve as suitable partners in cross-coupling reactions of (activated) secondary alkyl electrophiles. Thus, the first catalytic method for coupling secondary α-bromoketones with alkenylmetal reagents has been developed, specifically, a mild, versatile, and stereoconvergent carbon−carbon bond-forming process that generates potentially labile β,γ-unsaturated ketones with good enantioselectivity.en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (grant R01-GM62871)en_US
dc.description.sponsorshipNovartis (Firm)en_US
dc.description.sponsorshipMerck Research Laboratoriesen_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp:/dx.doi.org/10.1021/ja1017046en_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.sourceProf. Fuen_US
dc.titleEnantioselective Alkenylation via Nickel-Catalyzed Cross-Coupling with Organozirconium Reagentsen_US
dc.typeArticleen_US
dc.identifier.citationLou, Sha, and Gregory C. Fu. “Enantioselective Alkenylation via Nickel-Catalyzed Cross-Coupling with Organozirconium Reagents.” Journal of the American Chemical Society 132.14 (2010) : 5010-5011.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverFu, Gregory C.
dc.contributor.mitauthorLou, Sha
dc.contributor.mitauthorFu, Gregory C.
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.orderedauthorsLou, Sha; Fu, Gregory C.en
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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