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 *

121 related articles for article (PubMed ID: 25711834)

  • 1. Engaging nonaromatic, heterocyclic tosylates in reductive cross-coupling with aryl and heteroaryl bromides.
    Molander GA; Traister KM; O'Neill BT
    J Org Chem; 2015 Mar; 80(5):2907-11. PubMed ID: 25711834
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reductive cross-coupling of nonaromatic, heterocyclic bromides with aryl and heteroaryl bromides.
    Molander GA; Traister KM; O'Neill BT
    J Org Chem; 2014 Jun; 79(12):5771-80. PubMed ID: 24892751
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Copper-catalyzed reductive cross-coupling of nonactivated alkyl tosylates and mesylates with alkyl and aryl bromides.
    Liu JH; Yang CT; Lu XY; Zhang ZQ; Xu L; Cui M; Lu X; Xiao B; Fu Y; Liu L
    Chemistry; 2014 Nov; 20(47):15334-8. PubMed ID: 25308802
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Copper-catalyzed cross-coupling of aryl-, primary alkyl-, and secondary alkylboranes with heteroaryl bromides.
    Bergmann AM; Oldham AM; You W; Brown MK
    Chem Commun (Camb); 2018 May; 54(42):5381-5384. PubMed ID: 29745398
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Highly nucleophilic vitamin B
    Komeyama K; Ohata R; Kiguchi S; Osaka I
    Chem Commun (Camb); 2017 Jun; 53(48):6401-6404. PubMed ID: 28447093
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nickel-catalyzed methylation of aryl halides/tosylates with methyl tosylate.
    Wang J; Zhao J; Gong H
    Chem Commun (Camb); 2017 Sep; 53(73):10180-10183. PubMed ID: 28852757
    [TBL] [Abstract][Full Text] [Related]  

  • 7. NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acids.
    Percec V; Golding GM; Smidrkal J; Weichold O
    J Org Chem; 2004 May; 69(10):3447-52. PubMed ID: 15132555
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalyst.
    Hadei N; Kantchev EA; O'Brien CJ; Organ MG
    J Org Chem; 2005 Oct; 70(21):8503-7. PubMed ID: 16209599
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the negishi reaction: a step towards a universal cross-coupling catalyst.
    Organ MG; Avola S; Dubovyk I; Hadei N; Kantchev EA; O'Brien CJ; Valente C
    Chemistry; 2006 Jun; 12(18):4749-55. PubMed ID: 16568493
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nickel-catalyzed monofluoromethylation of (hetero)aryl bromides via reductive cross-coupling.
    Yin H; Sheng J; Zhang KF; Zhang ZQ; Bian KJ; Wang XS
    Chem Commun (Camb); 2019 Jul; 55(53):7635-7638. PubMed ID: 31198913
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Oxidative addition of aryl tosylates to palladium(0) and coupling of unactivated aryl tosylates at room temperature.
    Roy AH; Hartwig JF
    J Am Chem Soc; 2003 Jul; 125(29):8704-5. PubMed ID: 12862447
    [TBL] [Abstract][Full Text] [Related]  

  • 14. trans-Chloro(1-naphthyl)bis(triphenylphosphine)nickel(II)/PCy3 catalyzed cross-coupling of aryl and heteroaryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates at room temperature.
    Leowanawat P; Zhang N; Safi M; Hoffman DJ; Fryberger MC; George A; Percec V
    J Org Chem; 2012 Mar; 77(6):2885-92. PubMed ID: 22369478
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis of heteroaryl compounds through cross-coupling reaction of aryl bromides or benzyl halides with thienyl and pyridyl aluminum reagents.
    Chen X; Zhou L; Li Y; Xie T; Zhou S
    J Org Chem; 2014 Jan; 79(1):230-9. PubMed ID: 24308858
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Desulfonylative Arylation of Redox-Active Alkyl Sulfones with Aryl Bromides.
    Hughes JME; Fier PS
    Org Lett; 2019 Jul; 21(14):5650-5654. PubMed ID: 31273985
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heteroaromatic sulfonates and phosphates as electrophiles in iron-catalyzed cross-couplings.
    Gøgsig TM; Lindhardt AT; Skrydstrup T
    Org Lett; 2009 Nov; 11(21):4886-8. PubMed ID: 19785390
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Iron-catalysed, hydride-mediated reductive cross-coupling of vinyl halides and Grignard reagents.
    Le Bailly BA; Greenhalgh MD; Thomas SP
    Chem Commun (Camb); 2012 Feb; 48(10):1580-2. PubMed ID: 22041712
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Generation of Diversity Sets with High sp
    Raynor KD; May GD; Bandarage UK; Boyd MJ
    J Org Chem; 2018 Feb; 83(3):1551-1557. PubMed ID: 29281285
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nickel-mediated inter- and intramolecular reductive cross-coupling of unactivated alkyl bromides and aryl iodides at room temperature.
    Yan CS; Peng Y; Xu XB; Wang YW
    Chemistry; 2012 May; 18(19):6039-48. PubMed ID: 22473912
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.