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549 related items for PubMed ID: 15787581

  • 1. Efficient Stille cross-coupling reaction catalyzed by the Pd(OAc)2/Dabco catalytic system.
    Li JH, Liang Y, Wang DP, Liu WJ, Xie YX, Yin DL.
    J Org Chem; 2005 Apr 01; 70(7):2832-4. PubMed ID: 15787581
    [Abstract] [Full Text] [Related]

  • 2. Recyclable and reusable Pd(OAc)2/DABCO/PEG-400 system for Suzuki-Miyaura cross-coupling reaction.
    Li JH, Liu WJ, Xie YX.
    J Org Chem; 2005 Jul 08; 70(14):5409-12. PubMed ID: 15989320
    [Abstract] [Full Text] [Related]

  • 3. Dabco as an inexpensive and highly efficient ligand for palladium-catalyzed Suzuki-Miyaura cross-coupling reaction.
    Li JH, Liu WJ.
    Org Lett; 2004 Aug 05; 6(16):2809-11. PubMed ID: 15281775
    [Abstract] [Full Text] [Related]

  • 4. Guanidine/Pd(OAc)2-catalyzed room temperature Suzuki cross-coupling reaction in aqueous media under aerobic conditions.
    Li S, Lin Y, Cao J, Zhang S.
    J Org Chem; 2007 May 25; 72(11):4067-72. PubMed ID: 17465565
    [Abstract] [Full Text] [Related]

  • 5. Efficient palladium-catalyzed homocoupling reaction and Sonogashira cross-coupling reaction of terminal alkynes under aerobic conditions.
    Li JH, Liang Y, Xie YX.
    J Org Chem; 2005 May 27; 70(11):4393-6. PubMed ID: 15903317
    [Abstract] [Full Text] [Related]

  • 6. Pd(PPh3)4-PEG 400 catalyzed protocol for the atom-efficient Stille cross-coupling reaction of organotin with aryl bromides.
    Zhou WJ, Wang KH, Wang JX.
    J Org Chem; 2009 Aug 07; 74(15):5599-602. PubMed ID: 19552378
    [Abstract] [Full Text] [Related]

  • 7. CuI-catalyzed suzuki-miyaura and sonogashira cross-coupling reactions using DABCO as ligand.
    Li JH, Li JL, Wang DP, Pi SF, Xie YX, Zhang MB, Hu XC.
    J Org Chem; 2007 Mar 16; 72(6):2053-7. PubMed ID: 17286440
    [Abstract] [Full Text] [Related]

  • 8. (t-Bu)2PN=P(i-BuNCH2CH2)3N: new efficient ligand for palladium-catalyzed C-N couplings of aryl and heteroaryl bromides and chlorides and for vinyl bromides at room temperature.
    Reddy ChV, Kingston JV, Verkade JG.
    J Org Chem; 2008 Apr 18; 73(8):3047-62. PubMed ID: 18370424
    [Abstract] [Full Text] [Related]

  • 9. Synthesis of biaryls via decarboxylative Pd-catalyzed cross-coupling reaction.
    Becht JM, Catala C, Drian CL, Wagner A.
    Org Lett; 2007 Apr 26; 9(9):1781-3. PubMed ID: 17411063
    [Abstract] [Full Text] [Related]

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  • 11. Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).
    Terao J, Kambe N.
    Acc Chem Res; 2008 Nov 18; 41(11):1545-54. PubMed ID: 18973349
    [Abstract] [Full Text] [Related]

  • 12. 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. Reusable copper-catalyzed cross-coupling reactions of aryl halides with organotins in inexpensive ionic liquids.
    Li JH, Tang BX, Tao LM, Xie YX, Liang Y, Zhang MB.
    J Org Chem; 2006 Sep 15; 71(19):7488-90. PubMed ID: 16958550
    [Abstract] [Full Text] [Related]

  • 15. Highly active palladium catalysts supported by bulky proazaphosphatrane ligands for Stille cross-coupling: coupling of aryl and vinyl chlorides, room temperature coupling of aryl bromides, coupling of aryl triflates, and synthesis of sterically hindered biaryls.
    Su W, Urgaonkar S, McLaughlin PA, Verkade JG.
    J Am Chem Soc; 2004 Dec 22; 126(50):16433-9. PubMed ID: 15600345
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  • 17. Highly efficient, general procedure for the preparation of alkylzinc reagents from unactivated alkyl bromides and chlorides.
    Huo S.
    Org Lett; 2003 Feb 20; 5(4):423-5. PubMed ID: 12583734
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  • 19. Cross-coupling reactions of (1-fluorovinyl)methydiphenylsilane(1) with aryl halides and aryl triflates.
    Hanamoto T, Kobayashi T.
    J Org Chem; 2003 Aug 08; 68(16):6354-9. PubMed ID: 12895071
    [Abstract] [Full Text] [Related]

  • 20. Novel class of tertiary phosphine ligands based on a phospha-adamantane framework and use in the Suzuki cross-coupling reactions of aryl halides under mild conditions.
    Adjabeng G, Brenstrum T, Wilson J, Frampton C, Robertson A, Hillhouse J, McNulty J, Capretta A.
    Org Lett; 2003 Mar 20; 5(6):953-5. PubMed ID: 12633114
    [Abstract] [Full Text] [Related]

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