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dc.contributor.authorDooleweerdt, Karin
dc.contributor.authorFors, Brett P.
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2012-07-31T13:39:58Z
dc.date.available2012-07-31T13:39:58Z
dc.date.issued2010-04
dc.date.submitted2010-03
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.urihttp://hdl.handle.net/1721.1/71908
dc.description.abstractA catalyst, based on a biarylphosphine ligand, for the Pd-catalyzed cross-coupling reactions of amides and aryl mesylates is described. This system allows an array of aryl and heteroaryl mesylates to be transformed into the corresponding N-aryl amides in moderate to excellent yields.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant Number GM-58160)en_US
dc.description.sponsorshipHarvard University . BASF Advanced Research Initiativeen_US
dc.description.sponsorshipMerck Company Foundationen_US
dc.description.sponsorshipChemetallen_US
dc.description.sponsorshipNippon Chemical Industrial Co.en_US
dc.description.sponsorshipBoehringer Ingelheim Pharmaceuticals. Fellowshipen_US
dc.description.sponsorshipMerck Company Foundation. Fellowshipen_US
dc.description.sponsorshipUniversity of Aarhus. Department of Chemistryen_US
dc.description.sponsorshipUniversity of Aarhus. Interdisciplinary Nanoscience Centreen_US
dc.description.sponsorshipNational Science Foundation (Grant Number CHE 9808061)en_US
dc.description.sponsorshipNational Science Foundation (Grant Number DBI 9729592)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol100720xen_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.titlePd-Catalyzed Cross-Coupling Reactions of Amides and Aryl Mesylatesen_US
dc.typeArticleen_US
dc.identifier.citationDooleweerdt, Karin, Brett P. Fors, and Stephen L. Buchwald. “Pd-Catalyzed Cross-Coupling Reactions of Amides and Aryl Mesylates.” Organic Letters 12.10 (2010): 2350–2353.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverBuchwald, Stephen L.
dc.contributor.mitauthorDooleweerdt, Karin
dc.contributor.mitauthorFors, Brett P.
dc.contributor.mitauthorBuchwald, Stephen Leffler
dc.relation.journalOrganic Lettersen_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.orderedauthorsDooleweerdt, Karin; Fors, Brett P.; Buchwald, Stephen L.en
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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