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dc.contributor.authorZhu, Ye
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2015-04-09T18:29:18Z
dc.date.available2015-04-09T18:29:18Z
dc.date.issued2014-03
dc.date.submitted2014-02
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/96508
dc.description.abstractA palladium-catalyzed asymmetric arylation of 9-aminofluorene-derived imines using a chiral dialkylbiaryl phosphine as the supporting ligand has been developed. This transformation allows for enantioselective access to a diverse range of α-branched benzylamines.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Award GM58160)en_US
dc.description.sponsorshipAmgen Inc.en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ja501560xen_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.sourceAmerican Chemical Societyen_US
dc.titleLigand-Controlled Asymmetric Arylation of Aliphatic α-Amino Anion Equivalentsen_US
dc.typeArticleen_US
dc.identifier.citationZhu, Ye, and Stephen L. Buchwald. “Ligand-Controlled Asymmetric Arylation of Aliphatic α-Amino Anion Equivalents.” Journal of the American Chemical Society 136, no. 12 (March 26, 2014): 4500–4503. © 2014 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorBuchwald, Stephen Leffleren_US
dc.contributor.mitauthorZhu, Yeen_US
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
dspace.orderedauthorsZhu, Ye; Buchwald, Stephen L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8566-576X
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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