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 *

141 related articles for article (PubMed ID: 29869657)

  • 1. Acetylacetonato-based pincer-type nickel(ii) complexes: synthesis and catalysis in cross-couplings of aryl chlorides with aryl Grignard reagents.
    Asano E; Hatayama Y; Kurisu N; Ohtani A; Hashimoto T; Kurihara Y; Ueda K; Ishihara S; Nagao H; Yamaguchi Y
    Dalton Trans; 2018 Jun; 47(24):8003-8012. PubMed ID: 29869657
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ionic Ni(II) complexes containing a triphenylphosphine ligand and an imidazolium cation: synthesis, structures and catalysis for aryl Grignard cross-coupling of aryl halides.
    Xu YC; Zhang J; Sun HM; Shen Q; Zhang Y
    Dalton Trans; 2013 Jun; 42(23):8437-45. PubMed ID: 23624829
    [TBL] [Abstract][Full Text] [Related]  

  • 3. P,N,N-pincer nickel-catalyzed cross-coupling of aryl fluorides and chlorides.
    Wu D; Wang ZX
    Org Biomol Chem; 2014 Sep; 12(33):6414-24. PubMed ID: 25012049
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kumada coupling of aryl, heteroaryl, and vinyl chlorides catalyzed by amido pincer nickel complexes.
    Liu N; Wang ZX
    J Org Chem; 2011 Dec; 76(24):10031-8. PubMed ID: 22077596
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional group tolerant Kumada-Corriu-Tamao coupling of nonactivated alkyl halides with aryl and heteroaryl nucleophiles: catalysis by a nickel pincer complex permits the coupling of functionalized Grignard reagents.
    Vechorkin O; Proust V; Hu X
    J Am Chem Soc; 2009 Jul; 131(28):9756-66. PubMed ID: 19552426
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nickamine and Analogous Nickel Pincer Catalysts for Cross-Coupling of Alkyl Halides and Hydrosilylation of Alkenes.
    Shi R; Zhang Z; Hu X
    Acc Chem Res; 2019 May; 52(5):1471-1483. PubMed ID: 31008581
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cross-Coupling Reaction of Allylic Ethers with Aryl Grignard Reagents Catalyzed by a Nickel Pincer Complex.
    Hashimoto T; Funatsu K; Ohtani A; Asano E; Yamaguchi Y
    Molecules; 2019 Jun; 24(12):. PubMed ID: 31234296
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cross-Couplings Using Aryl Ethers via C-O Bond Activation Enabled by Nickel Catalysts.
    Tobisu M; Chatani N
    Acc Chem Res; 2015 Jun; 48(6):1717-26. PubMed ID: 26036674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nickel(II) complexes of bidentate N-heterocyclic carbene/phosphine ligands: efficient catalysts for Suzuki coupling of aryl chlorides.
    Lee CC; Ke WC; Chan KT; Lai CL; Hu CH; Lee HM
    Chemistry; 2007; 13(2):582-91. PubMed ID: 16969780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Nickel complexes supported by quinoline-based ligands: synthesis, characterization and catalysis in the cross-coupling of arylzinc reagents and aryl chlorides or aryltrimethylammonium salts.
    Zhang Q; Zhang XQ; Wang ZX
    Dalton Trans; 2012 Sep; 41(34):10453-64. PubMed ID: 22821185
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Activation of Aryl Halides by Nickel(I) Pincer Complexes: Reaction Pathways of Stoichiometric and Catalytic Dehalogenations.
    Rettenmeier CA; Wenz J; Wadepohl H; Gade LH
    Inorg Chem; 2016 Aug; 55(16):8214-24. PubMed ID: 27483018
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cross coupling of non-activated alkyl halides by a nickel pincer complex.
    Hu X
    Chimia (Aarau); 2010; 64(4):231-4. PubMed ID: 21138188
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Efficient cross-coupling of aryl chlorides with arylzinc reagents catalyzed by amido pincer complexes of nickel.
    Wang L; Wang ZX
    Org Lett; 2007 Oct; 9(21):4335-8. PubMed ID: 17887695
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hydroxyphosphine ligand for nickel-catalyzed cross-coupling through nickel/magnesium bimetallic cooperation.
    Yoshikai N; Matsuda H; Nakamura E
    J Am Chem Soc; 2009 Jul; 131(27):9590-9. PubMed ID: 19522507
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nickel-catalyzed coupling reaction of alkyl halides with aryl Grignard reagents in the presence of 1,3-butadiene: mechanistic studies of four-component coupling and competing cross-coupling reactions.
    Iwasaki T; Fukuoka A; Yokoyama W; Min X; Hisaki I; Yang T; Ehara M; Kuniyasu H; Kambe N
    Chem Sci; 2018 Feb; 9(8):2195-2211. PubMed ID: 29719693
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis of Cp*CH2PPh2 and its use as a ligand for the nickel-catalysed cross-coupling reaction of alkyl halides with aryl Grignard reagents.
    Uemura M; Yorimitsu H; Oshima K
    Chem Commun (Camb); 2006 Dec; (45):4726-8. PubMed ID: 17109050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis of quinolinyl-based pincer copper(ii) complexes: an efficient catalyst system for Kumada coupling of alkyl chlorides and bromides with alkyl Grignard reagents.
    Pandiri H; Gonnade RG; Punji B
    Dalton Trans; 2018 Nov; 47(46):16747-16754. PubMed ID: 30427350
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes.
    Terao J; Watanabe H; Ikumi A; Kuniyasu H; Kambe N
    J Am Chem Soc; 2002 Apr; 124(16):4222-3. PubMed ID: 11960446
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A structure-activity study of Ni-catalyzed alkyl-alkyl Kumada coupling. Improved catalysts for coupling of secondary alkyl halides.
    Ren P; Vechorkin O; von Allmen K; Scopelliti R; Hu X
    J Am Chem Soc; 2011 May; 133(18):7084-95. PubMed ID: 21500782
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.