BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 34122976)

  • 1. N
    Akporji N; Thakore RR; Cortes-Clerget M; Andersen J; Landstrom E; Aue DH; Gallou F; Lipshutz BH
    Chem Sci; 2020 May; 11(20):5205-5212. PubMed ID: 34122976
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Facile Assembly of Modular-Type Phosphines for Tackling Modern Arylation Processes.
    Tse MH; Choy PY; Kwong FY
    Acc Chem Res; 2022 Dec; 55(24):3688-3705. PubMed ID: 36472355
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hexacationic Dendriphos ligands in the Pd-catalyzed Suzuki-Miyaura cross-coupling reaction: scope and mechanistic studies.
    Snelders DJ; van Koten G; Klein Gebbink RJ
    J Am Chem Soc; 2009 Aug; 131(32):11407-16. PubMed ID: 19639941
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Palladium/P,O-Ligand-Catalyzed Suzuki Cross-Coupling Reactions of Arylboronic Acids and Aryl Chlorides. Isolation and Structural Characterization of (P,O)-Pd(dba) Complex.
    Bei X; Turner HW; Weinberg WH; Guram AS; Petersen JL
    J Org Chem; 1999 Sep; 64(18):6797-6803. PubMed ID: 11674689
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rapid room temperature Buchwald-Hartwig and Suzuki-Miyaura couplings of heteroaromatic compounds employing low catalyst loadings.
    Navarro O; Marion N; Mei J; Nolan SP
    Chemistry; 2006 Jun; 12(19):5142-8. PubMed ID: 16628762
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A highly active catalytic system for Suzuki-Miyaura cross-coupling reactions of aryl and heteroaryl chlorides in water.
    Mao SL; Sun Y; Yu GA; Zhao C; Han ZJ; Yuan J; Zhu X; Yang Q; Liu SH
    Org Biomol Chem; 2012 Dec; 10(47):9410-7. PubMed ID: 23111458
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An indole-amide-based phosphine ligand enabling a general palladium-catalyzed sterically hindered Suzuki-Miyaura cross-coupling reaction.
    Ng SS; Chen Z; Yuen OY; So CM
    Org Biomol Chem; 2022 Feb; 20(7):1373-1378. PubMed ID: 35080549
    [TBL] [Abstract][Full Text] [Related]  

  • 8. "Homeopathic" palladium nanoparticle catalysis of cross carbon-carbon coupling reactions.
    Deraedt C; Astruc D
    Acc Chem Res; 2014 Feb; 47(2):494-503. PubMed ID: 24215156
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Efficient catalyst for the Suzuki-Miyaura coupling of potassium aryl trifluoroborates with aryl chlorides.
    Barder TE; Buchwald SL
    Org Lett; 2004 Aug; 6(16):2649-52. PubMed ID: 15281735
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sustainable Ligand-Free, Palladium-Catalyzed Suzuki-Miyaura Reactions in Water: Insights into the Role of Base.
    Wang Y; Liu Y; Zhang WQ; Sun H; Zhang K; Jian Y; Gu Q; Zhang G; Li J; Gao Z
    ChemSusChem; 2019 Dec; 12(24):5265-5273. PubMed ID: 31724806
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A new,
    Takale BS; Thakore RR; Handa S; Gallou F; Reilly J; Lipshutz BH
    Chem Sci; 2019 Oct; 10(38):8825-8831. PubMed ID: 31803456
    [TBL] [Abstract][Full Text] [Related]  

  • 12. HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature.
    Handa S; Andersson MP; Gallou F; Reilly J; Lipshutz BH
    Angew Chem Int Ed Engl; 2016 Apr; 55(16):4914-8. PubMed ID: 26924396
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An active, general, and long-lived palladium catalyst for cross-couplings of deactivated (hetero)aryl chlorides and bromides with arylboronic acids.
    Hoshi T; Honma T; Mori A; Konishi M; Sato T; Hagiwara H; Suzuki T
    J Org Chem; 2013 Nov; 78(22):11513-24. PubMed ID: 24161157
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Suzuki-Miyaura coupling of aryl tosylates catalyzed by an array of indolyl phosphine-palladium catalysts.
    So CM; Lau CP; Chan AS; Kwong FY
    J Org Chem; 2008 Oct; 73(19):7731-4. PubMed ID: 18783275
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 9-fluorenylphosphines for the Pd-catalyzed sonogashira, suzuki, and Buchwald-Hartwig coupling reactions in organic solvents and water.
    Fleckenstein CA; Plenio H
    Chemistry; 2007; 13(9):2701-16. PubMed ID: 17200923
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis and Catalytic Applications of a Triptycene-Based Monophosphine Ligand for Palladium-Mediated Organic Transformations.
    Leung FK; Ishiwari F; Shoji Y; Nishikawa T; Takeda R; Nagata Y; Suginome M; Uozumi Y; Yamada YMA; Fukushima T
    ACS Omega; 2017 May; 2(5):1930-1937. PubMed ID: 31457552
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors.
    Jin B; Gallou F; Reilly J; Lipshutz BH
    Chem Sci; 2019 Mar; 10(12):3481-3485. PubMed ID: 30996938
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A General Palladium-Catalyzed Hiyama Cross-Coupling Reaction of Aryl and Heteroaryl Chlorides.
    Yuen OY; So CM; Man HW; Kwong FY
    Chemistry; 2016 May; 22(19):6471-6. PubMed ID: 26998586
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pd-catalyzed Suzuki-Miyaura reactions of aryl halides using bulky biarylmonophosphine ligands.
    Altman RA; Buchwald SL
    Nat Protoc; 2007; 2(12):3115-21. PubMed ID: 18079711
    [TBL] [Abstract][Full Text] [Related]  

  • 20. (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; 73(8):3047-62. PubMed ID: 18370424
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.