BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 34734604)

  • 1. Selective synthesis of enol ethers
    Gong L; Zhang Q; Xie D; Zhang W; Xu SY; Zhang X; Niu D
    Chem Commun (Camb); 2021 Nov; 57(92):12273-12276. PubMed ID: 34734604
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ni-Catalyzed Suzuki-Miyaura Cross-Coupling of α-Oxo-vinylsulfones To Prepare C-Aryl Glycals and Acyclic Vinyl Ethers.
    Gong L; Sun HB; Deng LF; Zhang X; Liu J; Yang S; Niu D
    J Am Chem Soc; 2019 May; 141(19):7680-7686. PubMed ID: 31025860
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dialkyl Ether Formation by Nickel-Catalyzed Cross-Coupling of Acetals and Aryl Iodides.
    Arendt KM; Doyle AG
    Angew Chem Int Ed Engl; 2015 Aug; 54(34):9876-80. PubMed ID: 26219537
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters.
    Tollefson EJ; Hanna LE; Jarvo ER
    Acc Chem Res; 2015 Aug; 48(8):2344-53. PubMed ID: 26197033
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Catalytic enantioselective cross-couplings of secondary alkyl electrophiles with secondary alkylmetal nucleophiles: Negishi reactions of racemic benzylic bromides with achiral alkylzinc reagents.
    Binder JT; Cordier CJ; Fu GC
    J Am Chem Soc; 2012 Oct; 134(41):17003-6. PubMed ID: 23039358
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nickel catalyzed dealkoxylative C(sp2)-C(sp3) cross coupling reactions--stereospecific synthesis of allylsilanes from enol ethers.
    Guo L; Leiendecker M; Hsiao CC; Baumann C; Rueping M
    Chem Commun (Camb); 2015 Feb; 51(10):1937-40. PubMed ID: 25532100
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exploration of new C-O electrophiles in cross-coupling reactions.
    Yu DG; Li BJ; Shi ZJ
    Acc Chem Res; 2010 Dec; 43(12):1486-95. PubMed ID: 20849101
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Direct Enol Ether Metalation-Negishi Coupling Strategy To Prepare α-Heteroaryl Enol Ethers.
    Peng F; Liu K; Zhang H; Xu F; Liu Y; Shang G
    Org Lett; 2023 Dec; 25(47):8516-8519. PubMed ID: 38037392
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nickel-catalyzed Negishi alkylations of styrenyl aziridines.
    Huang CY; Doyle AG
    J Am Chem Soc; 2012 Jun; 134(23):9541-4. PubMed ID: 22414150
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Decarbonylative Cross-Couplings: Nickel Catalyzed Functional Group Interconversion Strategies for the Construction of Complex Organic Molecules.
    Guo L; Rueping M
    Acc Chem Res; 2018 May; 51(5):1185-1195. PubMed ID: 29652129
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Efficient Synthesis of Diaryl Ketones by Nickel-Catalyzed Negishi Cross-Coupling of Amides by Carbon-Nitrogen Bond Cleavage at Room Temperature Accelerated by a Solvent Effect.
    Shi S; Szostak M
    Chemistry; 2016 Jul; 22(30):10420-4. PubMed ID: 27304392
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 2,2-difluorovinyl benzoates for diverse synthesis of gem-difluoroenol ethers by Ni-catalyzed cross-coupling reactions.
    Du B; Chan CM; Lee PY; Cheung LH; Xu X; Lin Z; Yu WY
    Nat Commun; 2021 Jan; 12(1):412. PubMed ID: 33462244
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Access to β-Ketonitriles through Nickel-Catalyzed Carbonylative Coupling of α-Bromonitriles with Alkylzinc Reagents.
    Donslund AS; Neumann KT; Corneliussen NP; Grove EK; Herbstritt D; Daasbjerg K; Skrydstrup T
    Chemistry; 2019 Jul; 25(42):9856-9860. PubMed ID: 31162751
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nickel-Catalyzed Reductive Conjugate Addition of Primary Alkyl Bromides to Enones To Form Silyl Enol Ethers.
    Huihui KM; Shrestha R; Weix DJ
    Org Lett; 2017 Jan; 19(2):340-343. PubMed ID: 28054785
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the chemical space of enol silyl ethers: catalytic dicarbofunctionalization enabled by iron catalysis.
    Sar D; Yin S; Grygus J; Rentería-Gómez Á; Garcia M; Gutierrez O
    Chem Sci; 2023 Nov; 14(45):13007-13013. PubMed ID: 38023494
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nickel-Catalyzed Reductive 2-Pyridination of Aryl Iodides with Difluoromethyl 2-Pyridyl Sulfone.
    Miao W; Ni C; Xiao P; Jia R; Zhang W; Hu J
    Org Lett; 2021 Feb; 23(3):711-715. PubMed ID: 33417469
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C-O Bond Activation.
    Tobisu M; Chatani N
    Top Curr Chem (Cham); 2016 Aug; 374(4):41. PubMed ID: 27573393
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Selective iron-catalyzed cross-coupling reactions of grignard reagents with enol triflates, acid chlorides, and dichloroarenes.
    Scheiper B; Bonnekessel M; Krause H; Fürstner A
    J Org Chem; 2004 May; 69(11):3943-9. PubMed ID: 15153029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bench-Stable Electrophilic Fluorinating Reagents for Highly Selective Mono- and Difluorination of Silyl Enol Ethers.
    Adachi A; Aikawa K; Ishibashi Y; Nozaki K; Okazoe T
    Chemistry; 2021 Aug; 27(46):11919-11925. PubMed ID: 34009678
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.