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 *

148 related articles for article (PubMed ID: 37070242)

  • 21. Nickel-Catalyzed Cross-Electrophile 1,2-Silyl-Arylation of 1,3-Dienes with Chlorosilanes and Aryl Bromides.
    Pan QQ; Qi L; Pang X; Shu XZ
    Angew Chem Int Ed Engl; 2023 Jan; 62(4):e202215703. PubMed ID: 36428246
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Visible-light induced cross-electrophile coupling of imines and anhydrides to synthesize α-amino ketones.
    Cao R; Liu Y; Shi X; Zheng J
    Chem Commun (Camb); 2023 Aug; 59(71):10668-10671. PubMed ID: 37581330
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Decarboxylative Cross-Electrophile Coupling of (Hetero)Aromatic Bromides and NHP Esters.
    DeCicco EM; Berritt S; Knauber T; Coffey SB; Hou J; Dowling MS
    J Org Chem; 2023 Sep; 88(17):12329-12340. PubMed ID: 37609685
    [TBL] [Abstract][Full Text] [Related]  

  • 24. B
    Pan M; Shen Y; Li Y; Shen C; Li W
    J Org Chem; 2024 Jun; 89(12):8656-8667. PubMed ID: 38831644
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Palladium-catalyzed cross-coupling of aziridinylmetal species, generated by sulfinyl-magnesium exchange, with aryl bromides: reaction optimization, scope, and kinetic investigations.
    Hughes M; Boultwood T; Zeppetelli G; Bull JA
    J Org Chem; 2013 Feb; 78(3):844-54. PubMed ID: 23311879
    [TBL] [Abstract][Full Text] [Related]  

  • 26. N-Aminopyridinium reagents as traceless activating groups in the synthesis of N-Aryl aziridines.
    Tan H; Samanta S; Maity A; Roychowdhury P; Powers DC
    Nat Commun; 2022 Jun; 13(1):3341. PubMed ID: 35689000
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chemoselective and Diastereoselective Synthesis of C-Aryl Nucleoside Analogues by Nickel-Catalyzed Cross-Coupling of Furanosyl Acetates with Aryl Iodides.
    Li Y; Wang Z; Li L; Tian X; Shao F; Li C
    Angew Chem Int Ed Engl; 2022 Jan; 61(1):e202110391. PubMed ID: 34664354
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Methods and Mechanisms for Cross-Electrophile Coupling of Csp(2) Halides with Alkyl Electrophiles.
    Weix DJ
    Acc Chem Res; 2015 Jun; 48(6):1767-75. PubMed ID: 26011466
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Electrochemical Reductive Cross-Coupling of Vinyl Bromides for the Synthesis of 1,3-Dienes.
    Zhang H; Ye Z; Wu Y; Zhang X; Ma W; Zhan ZJ; Zhang F
    Org Lett; 2024 Feb; 26(5):994-999. PubMed ID: 38289335
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Utilization of High-Throughput Experimentation (HTE) and ChemBeads Toward the Development of an Aryl Bromide and Benzyl Bromide Photoredox Cross-Electrophile Coupling.
    Glogowski MP; Cercizi N; Lynch-Colameta T; Ridgers LH; Phelan JP; Rowley AM; Rauch MP
    Org Lett; 2024 Mar; 26(12):2420-2424. PubMed ID: 38498905
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ligand-Controlled Nickel-Catalyzed Regiodivergent Cross-Electrophile Alkyl-Alkyl Couplings of Alkyl Halides.
    Zhao WT; Meng H; Lin JN; Shu W
    Angew Chem Int Ed Engl; 2023 Feb; 62(7):e202215779. PubMed ID: 36515409
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Stereoselective synthesis of trans- and cis-2-aryl-3-(hydroxymethyl)aziridines through transformation of 4-aryl-3-chloro-beta-lactams and study of their ring opening.
    D'hooghe M; Mollet K; Dekeukeleire S; De Kimpe N
    Org Biomol Chem; 2010 Feb; 8(3):607-15. PubMed ID: 20090977
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Nickel-Catalyzed Three-Component Cross-Electrophile Coupling of 1,3-Dienes with Aldehydes and Aryl Bromides.
    Qi YQ; Liu S; Xu Y; Li Y; Su T; Ni HL; Gao Y; Yu W; Cao P; Hu P; Zhao KQ; Wang BQ; Chen B
    Org Lett; 2022 Jul; 24(28):5023-5028. PubMed ID: 35822901
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Substrate-Mediator Duality of 1,4-Dicyanobenzene in Electrochemical C(sp
    Johnston B; Loh DM; Nocera DG
    Angew Chem Int Ed Engl; 2023 Dec; 62(49):e202312128. PubMed ID: 37857567
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Visible-Light-Induced Nickel-Catalyzed Radical Cross-Couplings to Access α-Aryl-α-trifluoromethyl Alcohols.
    Chen F; Xu XH; Chu L; Qing FL
    Org Lett; 2022 Dec; 24(50):9332-9336. PubMed ID: 36484514
    [TBL] [Abstract][Full Text] [Related]  

  • 37. General C(sp
    Truesdell BL; Hamby TB; Sevov CS
    J Am Chem Soc; 2020 Mar; 142(12):5884-5893. PubMed ID: 32115939
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Electroreductive Desulfurative Transformations with Thioethers as Alkyl Radical Precursors.
    Kuzmin J; Röckl J; Schwarz N; Djossou J; Ahumada G; Ahlquist M; Lundberg H
    Angew Chem Int Ed Engl; 2023 Sep; 62(39):e202304272. PubMed ID: 37342889
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Nickel-catalysed cross-electrophile coupling of aryl bromides and primary alkyl bromides.
    Gao N; Li Y; Teng D
    RSC Adv; 2022 Jan; 12(6):3569-3572. PubMed ID: 35425390
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Asymmetric Synthesis of β
    Takeda Y; Matsuno T; Sharma AK; Sameera WMC; Minakata S
    Chemistry; 2019 Aug; 25(43):10226-10231. PubMed ID: 31161639
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.