These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

498 related articles for article (PubMed ID: 15469301)

  • 1. 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]  

  • 2. Efficient synthesis of sterically crowded biaryls by palladium-phosphinous acid-catalyzed cross-coupling of aryl halides and aryl grignards.
    Wolf C; Xu H
    J Org Chem; 2008 Jan; 73(1):162-7. PubMed ID: 18052388
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of aryl chlorides.
    Hoshi T; Nakazawa T; Saitoh I; Mori A; Suzuki T; Sakai J; Hagiwara H
    Org Lett; 2008 May; 10(10):2063-6. PubMed ID: 18422322
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cross-coupling of diarylborinic acids and anhydrides with arylhalides catalyzed by a phosphite/N-heterocyclic carbene co-supported palladium catalyst system.
    Chen X; Ke H; Chen Y; Guan C; Zou G
    J Org Chem; 2012 Sep; 77(17):7572-8. PubMed ID: 22860711
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure.
    Barder TE; Walker SD; Martinelli JR; Buchwald SL
    J Am Chem Soc; 2005 Apr; 127(13):4685-96. PubMed ID: 15796535
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Palladium-catalyzed homocoupling and cross-coupling reactions of aryl halides in poly(ethylene glycol).
    Wang L; Zhang Y; Liu L; Wang Y
    J Org Chem; 2006 Feb; 71(3):1284-7. PubMed ID: 16438557
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Highly efficient monophosphine-based catalyst for the palladium-catalyzed suzuki-miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters.
    Billingsley K; Buchwald SL
    J Am Chem Soc; 2007 Mar; 129(11):3358-66. PubMed ID: 17326639
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pd-PEPPSI-IPent: low-temperature negishi cross-coupling for the preparation of highly functionalized, tetra-ortho-substituted biaryls.
    Calimsiz S; Sayah M; Mallik D; Organ MG
    Angew Chem Int Ed Engl; 2010 Mar; 49(11):2014-7. PubMed ID: 20162639
    [No Abstract]   [Full Text] [Related]  

  • 11. Scope and mechanism of palladium-catalyzed amination of five-membered heterocyclic halides.
    Hooper MW; Utsunomiya M; Hartwig JF
    J Org Chem; 2003 Apr; 68(7):2861-73. PubMed ID: 12662063
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cross-coupling reactions of arylsilanols with substituted aryl halides.
    Denmark SE; Ober MH
    Org Lett; 2003 Apr; 5(8):1357-60. PubMed ID: 12688758
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Palladium-catalyzed cross-coupling reactions of 2-indolyldimethylsilanols with substituted aryl halides.
    Denmark SE; Baird JD
    Org Lett; 2004 Sep; 6(20):3649-52. PubMed ID: 15387570
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sequential Ni-catalyzed borylation and cross-coupling of aryl halides via in situ prepared neopentylglycolborane.
    Rosen BM; Huang C; Percec V
    Org Lett; 2008 Jun; 10(12):2597-600. PubMed ID: 18484730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Palladium-phosphinous acid-catalyzed cross-coupling of aryl and acyl halides with aryl-, alkyl-, and vinylzinc reagents.
    Xu H; Ekoue-Kovi K; Wolf C
    J Org Chem; 2008 Oct; 73(19):7638-50. PubMed ID: 18767805
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Pd(μ-Cl)Cl(IPr*)]2: a highly hindered pre-catalyst for the synthesis of tetra-ortho-substituted biaryls via Grignard reagent cross-coupling.
    Lesieur M; Slawin AM; Cazin CS
    Org Biomol Chem; 2014 Aug; 12(30):5586-9. PubMed ID: 24967551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 41(11):1545-54. PubMed ID: 18973349
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Tetrasubstituted allenes by Pd0-catalyzed three-component tandem Michael addition/cross-coupling reaction.
    Xiao Y; Zhang J
    Chem Commun (Camb); 2010 Feb; 46(5):752-4. PubMed ID: 20087509
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The development of efficient catalysts for palladium-catalyzed coupling reactions of aryl halides.
    Zapf A; Beller M
    Chem Commun (Camb); 2005 Jan; (4):431-40. PubMed ID: 15654362
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.