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dc.contributor.authorSurry, David S.
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2015-02-11T15:17:15Z
dc.date.available2015-02-11T15:17:15Z
dc.date.issued2010-09
dc.date.submitted2010-06
dc.identifier.issn2041-6520
dc.identifier.issn2041-6539
dc.identifier.urihttp://hdl.handle.net/1721.1/94320
dc.description.abstractDialkylbiaryl phosphines are a valuable class of ligand for Pd-catalyzed amination reactions and have been applied in a range of contexts. This perspective attempts to aid the reader in the selection of the best choice of reaction conditions and ligand of this class for the most commonly encountered and practically important substrate combinations.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM-58160)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistry, Theen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c0sc00331jen_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.titleDialkylbiaryl phosphines in Pd-catalyzed amination: a user's guideen_US
dc.typeArticleen_US
dc.identifier.citationSurry, David S., and Stephen L. Buchwald. “Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: a User’s Guide.” Chemical Science 2, no. 1 (2010): 27.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorBuchwald, Stephen Leffleren_US
dc.contributor.mitauthorSurry, David S.en_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.orderedauthorsSurry, David S.; 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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