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dc.contributor.authorLou, Sha
dc.contributor.authorFu, Gregory C.
dc.date.accessioned2013-11-15T14:17:36Z
dc.date.available2013-11-15T14:17:36Z
dc.date.issued2010-07
dc.date.submitted2010-04
dc.identifier.issn16154150
dc.identifier.urihttp://hdl.handle.net/1721.1/82111
dc.description.abstractDipalladiumtris(dibenzylideneacetone)/tris(tert-butyl)phosphonium tetrafluoroborate/potassium fluoride dihydrate [Pd2(dba)3/[HP(t-Bu)3]BF4/KF⋅2 H2O] serves as a mild, robust, and user-friendly method for the efficient Suzuki cross-coupling of a diverse array of aryl and heteroaryl halides with aryl- and heteroarylboronic acids.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (National Institute of General Medical Sciences, grant R01-GM62871)en_US
dc.description.sponsorshipMerck Research Laboratoriesen_US
dc.description.sponsorshipNovartis (Firm)en_US
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/adsc.201000267en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titlePalladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Wateren_US
dc.typeArticleen_US
dc.identifier.citationLou, Sha, and Gregory C. Fu. “Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water.” Advanced Synthesis & Catalysis 352, no. 11 12 (October 9, 2010): 2081-2084.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorLou, Shaen_US
dc.contributor.mitauthorFu, Gregory C.en_US
dc.relation.journalAdvanced Synthesis & Catalysisen_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.orderedauthorsLou, Sha; Fu, Gregory C.en_US
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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