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 *

288 related articles for article (PubMed ID: 26023832)

  • 1. Alkyl-aryl ketone synthesis via nickel-catalyzed reductive coupling of alkyl halides with aryl acids and anhydrides.
    Jia X; Zhang X; Qian Q; Gong H
    Chem Commun (Camb); 2015 Jun; 51(51):10302-5. PubMed ID: 26023832
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mild ketone formation via Ni-catalyzed reductive coupling of unactivated alkyl halides with acid anhydrides.
    Yin H; Zhao C; You H; Lin K; Gong H
    Chem Commun (Camb); 2012 Jul; 48(56):7034-6. PubMed ID: 22684052
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ni-catalyzed reductive coupling of alkyl acids with unactivated tertiary alkyl and glycosyl halides.
    Zhao C; Jia X; Wang X; Gong H
    J Am Chem Soc; 2014 Dec; 136(50):17645-51. PubMed ID: 25415424
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ketone formation via mild nickel-catalyzed reductive coupling of alkyl halides with aryl acid chlorides.
    Wu F; Lu W; Qian Q; Ren Q; Gong H
    Org Lett; 2012 Jun; 14(12):3044-7. PubMed ID: 22651806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reductive Cross-Coupling of Unreactive Electrophiles.
    Pang X; Su PF; Shu XZ
    Acc Chem Res; 2022 Sep; 55(17):2491-2509. PubMed ID: 35951536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dual nickel- and photoredox-catalyzed reductive cross-coupling of aryl vinyl halides and unactivated tertiary alkyl bromides.
    Yu W; Chen L; Tao J; Wang T; Fu J
    Chem Commun (Camb); 2019 May; 55(42):5918-5921. PubMed ID: 31045192
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Nickel-Catalyzed Reductive Coupling of γ-Metalated Ketones with Unactivated Alkyl Bromides.
    Cui N; Lin T; Wang YE; Wu J; Han Y; Xu X; Xue F; Xiong D; Walsh PJ; Mao J
    Org Lett; 2022 Jun; 24(22):3987-3992. PubMed ID: 35639094
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Alkyl Bromides: Et3N as the Terminal Reductant.
    Duan Z; Li W; Lei A
    Org Lett; 2016 Aug; 18(16):4012-5. PubMed ID: 27472556
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Computational Insight into Nickel-Catalyzed Carbon-Carbon versus Carbon-Boron Coupling Reactions of Primary, Secondary, and Tertiary Alkyl Bromides.
    Cheung MS; Sheong FK; Marder TB; Lin Z
    Chemistry; 2015 May; 21(20):7480-8. PubMed ID: 25831999
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stereoselective Preparation of α- C-Vinyl/Aryl Glycosides via Nickel-Catalyzed Reductive Coupling of Glycosyl Halides with Vinyl and Aryl Halides.
    Liu J; Gong H
    Org Lett; 2018 Dec; 20(24):7991-7995. PubMed ID: 30525666
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Nickel-Catalyzed Reductive Coupling of Aryl Bromides with Tertiary Alkyl Halides.
    Wang X; Wang S; Xue W; Gong H
    J Am Chem Soc; 2015 Sep; 137(36):11562-5. PubMed ID: 26325479
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nickel-Catalyzed Direct Electrochemical Cross-Coupling between Aryl Halides and Activated Alkyl Halides.
    Durandetti M; Nédélec JY; Périchon J
    J Org Chem; 1996 Mar; 61(5):1748-1755. PubMed ID: 11667045
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ester Formation via Nickel-Catalyzed Reductive Coupling of Alkyl Halides with Chloroformates.
    Zheng M; Xue W; Xue T; Gong H
    Org Lett; 2016 Dec; 18(23):6152-6155. PubMed ID: 27934381
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ni-catalyzed enantioconvergent deoxygenative reductive cross-coupling of unactivated alkyl alcohols and aryl bromides.
    Zhang LL; Gao YZ; Cai SH; Yu H; Shen SJ; Ping Q; Yang ZP
    Nat Commun; 2024 Mar; 15(1):2733. PubMed ID: 38548758
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nickel-Catalyzed Reductive Thiolation of Unactivated Alkyl Bromides and Arenesulfonyl Cyanides.
    Wang F; Rao W; Wang SY
    J Org Chem; 2021 Jul; 86(13):8970-8979. PubMed ID: 34142832
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Cobalt-catalyzed reductive coupling of saturated alkyl halides with activated alkenes.
    Shukla P; Hsu YC; Cheng CH
    J Org Chem; 2006 Jan; 71(2):655-8. PubMed ID: 16408976
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides.
    Fang Y; Rogge T; Ackermann L; Wang SY; Ji SJ
    Nat Commun; 2018 Jun; 9(1):2240. PubMed ID: 29884782
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copper-Catalyzed Stereoselective Borylation and Palladium-Catalyzed Stereospecific Cross-Coupling to Give Aryl C-Glycosides.
    Kurahayashi K; Hanaya K; Sugai T; Hirai G; Higashibayashi S
    Chemistry; 2023 Jan; 29(6):e202203376. PubMed ID: 36344464
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.