BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 19441851)

  • 1. Negishi coupling of secondary alkylzinc halides with aryl bromides and chlorides.
    Han C; Buchwald SL
    J Am Chem Soc; 2009 Jun; 131(22):7532-3. PubMed ID: 19441851
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Simple, efficient catalyst system for the palladium-catalyzed amination of aryl chlorides, bromides, and triflates.
    Wolfe JP; Tomori H; Sadighi JP; Yin J; Buchwald SL
    J Org Chem; 2000 Feb; 65(4):1158-74. PubMed ID: 10814067
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pd-PEPPSI-IPent(Cl): a highly effective catalyst for the selective cross-coupling of secondary organozinc reagents.
    Pompeo M; Froese RD; Hadei N; Organ MG
    Angew Chem Int Ed Engl; 2012 Nov; 51(45):11354-7. PubMed ID: 23038603
    [TBL] [Abstract][Full Text] [Related]  

  • 4. AlAr3(THF): highly efficient reagents for cross-couplings with aryl bromides and chlorides catalyzed by the economic palladium complex of PCy3.
    Ku SL; Hui XP; Chen CA; Kuo YY; Gau HM
    Chem Commun (Camb); 2007 Oct; (37):3847-9. PubMed ID: 18217667
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates.
    Zhou J; Fu GC
    J Am Chem Soc; 2003 Oct; 125(41):12527-30. PubMed ID: 14531697
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 132(33):11592-8. PubMed ID: 20672810
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mild Negishi cross-coupling reactions catalyzed by acenaphthoimidazolylidene palladium complexes at low catalyst loadings.
    Liu Z; Dong N; Xu M; Sun Z; Tu T
    J Org Chem; 2013 Aug; 78(15):7436-44. PubMed ID: 23834110
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis of 2-arylpiperidines by palladium couplings of aryl bromides with organozinc species derived from deprotonation of N-boc-piperidine.
    Coldham I; Leonori D
    Org Lett; 2008 Sep; 10(17):3923-5. PubMed ID: 18683935
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ligand-free palladium-catalyzed direct arylation of thiazoles at low catalyst loadings.
    Roger J; Pozgan F; Doucet H
    J Org Chem; 2009 Feb; 74(3):1179-86. PubMed ID: 19133743
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nickel-catalyzed asymmetric cross-couplings of racemic propargylic halides with arylzinc reagents.
    Smith SW; Fu GC
    J Am Chem Soc; 2008 Sep; 130(38):12645-7. PubMed ID: 18763769
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Palladium-catalyzed decarboxylative coupling of alkynyl carboxylic acids and aryl halides.
    Moon J; Jang M; Lee S
    J Org Chem; 2009 Feb; 74(3):1403-6. PubMed ID: 19099411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Palladium-catalyzed intermolecular alpha-arylation of zinc amide enolates under mild conditions.
    Hama T; Culkin DA; Hartwig JF
    J Am Chem Soc; 2006 Apr; 128(15):4976-85. PubMed ID: 16608331
    [TBL] [Abstract][Full Text] [Related]  

  • 13. On the stereochemical course of palladium-catalyzed cross-coupling of allylic silanolate salts with aromatic bromides.
    Denmark SE; Werner NS
    J Am Chem Soc; 2010 Mar; 132(10):3612-20. PubMed ID: 20163185
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Highly selective palladium-catalyzed cross-coupling of secondary alkylzinc reagents with heteroaryl halides.
    Yang Y; Niedermann K; Han C; Buchwald SL
    Org Lett; 2014 Sep; 16(17):4638-41. PubMed ID: 25153332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Scope and limitations of the Pd/BINAP-catalyzed amination of aryl bromides.
    Wolfe JP; Buchwald SL
    J Org Chem; 2000 Feb; 65(4):1144-57. PubMed ID: 10814066
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nickel-catalyzed reductive coupling of aryl halides with secondary alkyl bromides and allylic acetate.
    Wang S; Qian Q; Gong H
    Org Lett; 2012 Jul; 14(13):3352-5. PubMed ID: 22697415
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Highly reactive, general, and long-lived catalysts for coupling heteroaryl and aryl chlorides with primary nitrogen nucleophiles.
    Shen Q; Shekhar S; Stambuli JP; Hartwig JF
    Angew Chem Int Ed Engl; 2005 Feb; 44(9):1371-5. PubMed ID: 15666413
    [No Abstract]   [Full Text] [Related]  

  • 18. Revealing a second transmetalation step in the Negishi coupling and its competition with reductive elimination: improvement in the interpretation of the mechanism of biaryl syntheses.
    Liu Q; Lan Y; Liu J; Li G; Wu YD; Lei A
    J Am Chem Soc; 2009 Jul; 131(29):10201-10. PubMed ID: 19572717
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An extremely active catalyst for the Negishi cross-coupling reaction.
    Milne JE; Buchwald SL
    J Am Chem Soc; 2004 Oct; 126(40):13028-32. PubMed ID: 15469301
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Palladium-catalyzed α-arylation of benzylic phosphine oxides.
    Montel S; Jia T; Walsh PJ
    Org Lett; 2014 Jan; 16(1):130-3. PubMed ID: 24295336
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.