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Journal Abstract Search

749 related items for PubMed ID: 15600345

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  • 6. Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides.
    Littke AF, Schwarz L, Fu GC.
    J Am Chem Soc; 2002 Jun 05; 124(22):6343-8. PubMed ID: 12033863
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  • 7. Aqueous-phase, palladium-catalyzed cross-coupling of aryl bromides under mild conditions, using water-soluble, sterically demanding alkylphosphines.
    DeVasher RB, Moore LR, Shaughnessy KH.
    J Org Chem; 2004 Nov 12; 69(23):7919-27. PubMed ID: 15527271
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  • 8. A general method for the Suzuki-Miyaura cross-coupling of sterically hindered aryl chlorides: synthesis of di- and tri-ortho-substituted biaryls in 2-propanol at room temperature.
    Navarro O, Kelly RA, Nolan SP.
    J Am Chem Soc; 2003 Dec 31; 125(52):16194-5. PubMed ID: 14692753
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  • 10. Orthopalladated and -platinated bulky triarylphosphite complexes: synthesis, reactivity and application as high-activity catalysts for Suzuki and Stille coupling reactions.
    Bedford RB, Hazelwood SL, Limmert ME, Albisson DA, Draper SM, Scully PN, Coles SJ, Hursthouse MB.
    Chemistry; 2003 Jul 21; 9(14):3216-27. PubMed ID: 12866065
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  • 12. Oxidative addition of aryl tosylates to palladium(0) and coupling of unactivated aryl tosylates at room temperature.
    Roy AH, Hartwig JF.
    J Am Chem Soc; 2003 Jul 23; 125(29):8704-5. PubMed ID: 12862447
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  • 13. Efficient Stille cross-coupling reaction using aryl chlorides or bromides in water.
    Wolf C, Lerebours R.
    J Org Chem; 2003 Sep 19; 68(19):7551-4. PubMed ID: 12968920
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  • 14. Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biaryls.
    Organ MG, Calimsiz S, Sayah M, Hoi KH, Lough AJ.
    Angew Chem Int Ed Engl; 2009 Sep 19; 48(13):2383-7. PubMed ID: 19226587
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  • 16. Homogeneous catalysts supported on soluble polymers: biphasic Sonogashira coupling of aryl halides and acetylenes using MeOPEG-bound phosphine-palladium catalysts for efficient catalyst recycling.
    Köllhofer A, Plenio H.
    Chemistry; 2003 Mar 17; 9(6):1416-25. PubMed ID: 12645031
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  • 17. Palladium-catalyzed aminations of aryl halides with phosphine-functionalized imidazolium ligands.
    Shi JC, Yang P, Tong Q, Jia L.
    Dalton Trans; 2008 Feb 21; (7):938-45. PubMed ID: 18259628
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  • 18. The development of versatile methods for palladium-catalyzed coupling reactions of aryl electrophiles through the use of P(t-Bu)3 and PCy3 as ligands.
    Fu GC.
    Acc Chem Res; 2008 Nov 18; 41(11):1555-64. PubMed ID: 18947239
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  • 20. Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of sterically hindered aryl bromides.
    Hoshi T, Saitoh I, Nakazawa T, Suzuki T, Sakai J, Hagiwara H.
    J Org Chem; 2009 May 15; 74(10):4013-6. PubMed ID: 19391580
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