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dc.contributor.authorMaiti, Debabrata
dc.contributor.authorFors, Brett P.
dc.contributor.authorHenderson, Jaclyn L.
dc.contributor.authorNakamura, Yoshinori
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2015-02-11T16:19:07Z
dc.date.available2015-02-11T16:19:07Z
dc.date.issued2010-09
dc.date.submitted2010-06
dc.identifier.issn2041-6520
dc.identifier.issn2041-6539
dc.identifier.urihttp://hdl.handle.net/1721.1/94326
dc.description.abstractWe report our studies on the use of two catalyst systems, based on the ligands BrettPhos and RuPhos, which provide the widest scope for Pd-catalyzed C–N cross-coupling reactions to date. Often low catalyst loadings and short reaction times can be used with functionalized aryl and heteroaryl coupling partners. The reactions are highly robust and can be set up and performed without the use of a glovebox. These catalysts should find wide application in the synthesis of complex molecules including pharmaceuticals, natural products and functional materials.en_US
dc.description.sponsorshipAmgen Inc.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM-58160)en_US
dc.description.sponsorshipAmerican Chemical Societyen_US
dc.description.sponsorshipBoehringer Ingelheimen_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CHE 9808061)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (DBI 9729592)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistry, Theen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c0sc00330aen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titlePalladium-catalyzed coupling of functionalized primary and secondary amines with aryl and heteroaryl halides: two ligands suffice in most casesen_US
dc.typeArticleen_US
dc.identifier.citationMaiti, Debabrata, Brett P. Fors, Jaclyn L. Henderson, Yoshinori Nakamura, and Stephen L. Buchwald. “Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases.” Chemical Science 2, no. 1 (2011): 57.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorMaiti, Debabrataen_US
dc.contributor.mitauthorFors, Brett P.en_US
dc.contributor.mitauthorHenderson, Jaclyn L.en_US
dc.contributor.mitauthorNakamura, Yoshinorien_US
dc.contributor.mitauthorBuchwald, Stephen Leffleren_US
dc.relation.journalChemical Scienceen_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.orderedauthorsMaiti, Debabrata; Fors, Brett P.; Henderson, Jaclyn L.; Nakamura, Yoshinori; Buchwald, Stephen L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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