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dc.contributor.authorFors, Brett P.
dc.contributor.authorDooleweerdt, Karin
dc.contributor.authorZeng, Qingle
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2015-10-28T12:51:22Z
dc.date.available2015-10-28T12:51:22Z
dc.date.issued2009-05
dc.date.submitted2009-04
dc.identifier.issn00404020
dc.identifier.urihttp://hdl.handle.net/1721.1/99484
dc.description.abstractA catalyst based on a new biarylphosphine ligand (3) for the Pd-catalyzed cross-coupling reactions of amides and aryl chlorides is described. This system shows the highest turnover frequencies reported to date for these reactions, especially for aryl chloride substrates bearing an ortho substituent. An array of amides and aryl chlorides were successfully reacted in good to excellent yields.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM-58160)en_US
dc.description.sponsorshipMerck & Co., Inc.en_US
dc.description.sponsorshipBASFen_US
dc.description.sponsorshipChemetallen_US
dc.description.sponsorshipNippon Chemical Industrial Co.en_US
dc.description.sponsorshipWilliam Asbornsen Albert Memorial Fund (Fellowship)en_US
dc.description.sponsorshipUniversity of Aarhus. Department of Chemistryen_US
dc.description.sponsorshipUniversity of Aarhus. Interdisciplinary Nanoscience Centreen_US
dc.description.sponsorshipChina Scholarship Councilen_US
dc.description.sponsorshipNational Natural Science Foundation (China) (Grant 20672088)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.tet.2009.04.096en_US
dc.rightsCreative Commons Attribution-Noncommercial-NoDerivativesen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleAn efficient system for the Pd-catalyzed cross-coupling of amides and aryl chloridesen_US
dc.typeArticleen_US
dc.identifier.citationFors, Brett P., Karin Dooleweerdt, Qingle Zeng, and Stephen L. Buchwald. “An Efficient System for the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.” Tetrahedron 65, no. 33 (August 2009): 6576–6583.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorFors, Brett P.en_US
dc.contributor.mitauthorDooleweerdt, Karinen_US
dc.contributor.mitauthorZeng, Qingleen_US
dc.contributor.mitauthorBuchwald, Stephen Leffleren_US
dc.relation.journalTetrahedronen_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.orderedauthorsFors, Brett P.; Dooleweerdt, Karin; Zeng, Qingle; Buchwald, Stephen L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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