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dc.contributor.authorLou, Sha
dc.contributor.authorFu, Gregory C.
dc.date.accessioned2011-12-14T14:39:18Z
dc.date.available2011-12-14T14:39:18Z
dc.date.issued2010-01
dc.identifier.issn0078-6209
dc.identifier.urihttp://hdl.handle.net/1721.1/67662
dc.description.abstractThe transition metal-catalyzed enantioselective coupling of allylic electrophiles with carbon nucleophiles has been the focus of intense investigation.5 Salient examples include palladium-catalyzed couplings with enolates, nickel-catalyzed couplings with Grignard reagents, and copper-catalyzed couplings with Grignard and diorganozinc reagents.6 Despite impressive progress, the development of methods that have broader scope with respect to the nucleophile, as well as improved functional-group compatibility, persist as important challenges.en_US
dc.language.isoen_US
dc.publisherOrganic Syntheses, Inc.en_US
dc.relation.isversionofhttp://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=v87p0317en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcejohansen@mit.eduen_US
dc.titleNickel-Catalyzed Asymmetric Negishi Cross-Couplings of Racemic Secondary Allylic Chlorides with Alkylzincsen_US
dc.typeArticleen_US
dc.identifier.citationLou, Sha, and Gregory C. Fu. “NICKEL-CATALYZED ASYMMETRIC NEGISHI CROSS-COUPLINGS OF RACEMIC SECONDARY ALLYLIC CHLORIDES WITH ALKYLZINCS: (S,E)-ETHYL 6-(1,3-DIOXOLAN-2-YL)-4-METHYLHEX-2-ENOATE.” Organic Syntheses 87 (2010) : 317.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.contributor.approverFu, Gregory C.
dc.contributor.mitauthorFu, Gregory C.
dc.contributor.mitauthorLou, Sha
dc.relation.journalOrganic Synthesesen_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_US
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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