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Journal Abstract Search

1402 related items for PubMed ID: 16536531

  • 21.
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  • 23. Efficient pd-catalyzed amination of heteroaryl halides.
    Charles MD, Schultz P, Buchwald SL.
    Org Lett; 2005 Sep 01; 7(18):3965-8. PubMed ID: 16119943
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  • 25. Palladium-catalyzed formylation of aryl bromides: elucidation of the catalytic cycle of an industrially applied coupling reaction.
    Sergeev AG, Spannenberg A, Beller M.
    J Am Chem Soc; 2008 Nov 19; 130(46):15549-63. PubMed ID: 18956867
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  • 26. Exploiting noninnocent (E,E)-dibenzylideneacetone (dba) effects in palladium(0)-mediated cross-coupling reactions: modulation of the electronic properties of dba affects catalyst activity and stability in ligand and ligand-free reaction systems.
    Fairlamb IJ, Kapdi AR, Lee AF, McGlacken GP, Weissburger F, de Vries AH, Schmieder-van de Vondervoort L.
    Chemistry; 2006 Nov 24; 12(34):8750-61. PubMed ID: 16952128
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  • 27. Palladium-catalyzed asymmetric phosphination. Scope, mechanism, and origin of enantioselectivity.
    Blank NF, Moncarz JR, Brunker TJ, Scriban C, Anderson BJ, Amir O, Glueck DS, Zakharov LN, Golen JA, Incarvito CD, Rheingold AL.
    J Am Chem Soc; 2007 May 30; 129(21):6847-58. PubMed ID: 17474744
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  • 29. Copper(I)-catalyzed amination of aryl halides in liquid ammonia.
    Ji P, Atherton JH, Page MI.
    J Org Chem; 2012 Sep 07; 77(17):7471-8. PubMed ID: 22849292
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  • 31. Synthetic, structural, and mechanistic studies on the oxidative addition of aromatic chlorides to a palladium (N-heterocyclic carbene) complex: relevance to catalytic amination.
    Lewis AK, Caddick S, Cloke FG, Billingham NC, Hitchcock PB, Leonard J.
    J Am Chem Soc; 2003 Aug 20; 125(33):10066-73. PubMed ID: 12914470
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  • 34. Identification of an activated catalyst in the iridium-catalyzed allylic amination and etherification. Increased rates, scope, and selectivity.
    Kiener CA, Shu C, Incarvito C, Hartwig JF.
    J Am Chem Soc; 2003 Nov 26; 125(47):14272-3. PubMed ID: 14624564
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  • 36. 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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  • 37. Preferential oxidative addition in palladium(0)-catalyzed suzuki cross-coupling reactions of dihaloarenes with arylboronic acids.
    Dong CG, Hu QS.
    J Am Chem Soc; 2005 Jul 20; 127(28):10006-7. PubMed ID: 16011357
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  • 38. Scope and mechanism of allylic C-H amination of terminal alkenes by the palladium/PhI(OPiv)2 catalyst system: insights into the effect of naphthoquinone.
    Yin G, Wu Y, Liu G.
    J Am Chem Soc; 2010 Sep 01; 132(34):11978-87. PubMed ID: 20690676
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  • 39. Palladium-catalyzed three-component coupling of arynes with allylic acetates or halides and terminal alkynes promoted by cuprous iodide.
    Bhuvaneswari S, Jeganmohan M, Yang MC, Cheng CH.
    Chem Commun (Camb); 2008 May 14; (18):2158-60. PubMed ID: 18438501
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  • 40. A general and efficient catalyst for palladium-catalyzed C-O coupling reactions of aryl halides with primary alcohols.
    Gowrisankar S, Sergeev AG, Anbarasan P, Spannenberg A, Neumann H, Beller M.
    J Am Chem Soc; 2010 Aug 25; 132(33):11592-8. PubMed ID: 20672810
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