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Journal Abstract Search

335 related items for PubMed ID: 28421708

  • 1. Control of Vicinal Stereocenters through Nickel-Catalyzed Alkyl-Alkyl Cross-Coupling.
    Mu X, Shibata Y, Makida Y, Fu GC.
    Angew Chem Int Ed Engl; 2017 May 15; 56(21):5821-5824. PubMed ID: 28421708
    [Abstract] [Full Text] [Related]

  • 2. Enantioconvergent Cross-Couplings of Alkyl Electrophiles: The Catalytic Asymmetric Synthesis of Organosilanes.
    Schwarzwalder GM, Matier CD, Fu GC.
    Angew Chem Int Ed Engl; 2019 Mar 11; 58(11):3571-3574. PubMed ID: 30650228
    [Abstract] [Full Text] [Related]

  • 3. Nickel-Catalyzed Enantioconvergent Borylation of Racemic Secondary Benzylic Electrophiles.
    Wang Z, Bachman S, Dudnik AS, Fu GC.
    Angew Chem Int Ed Engl; 2018 Oct 26; 57(44):14529-14532. PubMed ID: 30079625
    [Abstract] [Full Text] [Related]

  • 4. Stereoconvergent Negishi Arylations of Racemic Secondary Alkyl Electrophiles: Differentiating between a CF3 and an Alkyl Group.
    Liang Y, Fu GC.
    J Am Chem Soc; 2015 Aug 05; 137(30):9523-6. PubMed ID: 26203662
    [Abstract] [Full Text] [Related]

  • 5. Ni-Catalyzed C-C Couplings Using Alkyl Electrophiles.
    Iwasaki T, Kambe N.
    Top Curr Chem (Cham); 2016 Oct 05; 374(5):66. PubMed ID: 27580894
    [Abstract] [Full Text] [Related]

  • 6. Nickel-Catalyzed Alkyl-Alkyl Cross-Couplings of Fluorinated Secondary Electrophiles: A General Approach to the Synthesis of Compounds having a Perfluoroalkyl Substituent.
    Liang Y, Fu GC.
    Angew Chem Int Ed Engl; 2015 Jul 27; 54(31):9047-51. PubMed ID: 26073669
    [Abstract] [Full Text] [Related]

  • 7. New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles.
    Wilsily A, Tramutola F, Owston NA, Fu GC.
    J Am Chem Soc; 2012 Apr 04; 134(13):5794-7. PubMed ID: 22443409
    [Abstract] [Full Text] [Related]

  • 8. Reductive Cross-Coupling of Unreactive Electrophiles.
    Pang X, Su PF, Shu XZ.
    Acc Chem Res; 2022 Sep 06; 55(17):2491-2509. PubMed ID: 35951536
    [Abstract] [Full Text] [Related]

  • 9. Nickel-Catalyzed Stereoselective Coupling Reactions of Benzylic and Alkyl Alcohol Derivatives.
    Herbert CA, Jarvo ER.
    Acc Chem Res; 2023 Nov 21; 56(22):3313-3324. PubMed ID: 37936256
    [Abstract] [Full Text] [Related]

  • 10. Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters.
    Tollefson EJ, Hanna LE, Jarvo ER.
    Acc Chem Res; 2015 Aug 18; 48(8):2344-53. PubMed ID: 26197033
    [Abstract] [Full Text] [Related]

  • 11. 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 17; 134(41):17003-6. PubMed ID: 23039358
    [Abstract] [Full Text] [Related]

  • 12. Asymmetric Synthesis of Protected Unnatural α-Amino Acids via Enantioconvergent Nickel-Catalyzed Cross-Coupling.
    Yang ZP, Freas DJ, Fu GC.
    J Am Chem Soc; 2021 Jun 16; 143(23):8614-8618. PubMed ID: 34080836
    [Abstract] [Full Text] [Related]

  • 13. Nickel-catalyzed coupling reactions of alkyl electrophiles, including unactivated tertiary halides, to generate carbon-boron bonds.
    Dudnik AS, Fu GC.
    J Am Chem Soc; 2012 Jun 27; 134(25):10693-7. PubMed ID: 22668072
    [Abstract] [Full Text] [Related]

  • 14. Enantioselective alkyl-alkyl Suzuki cross-couplings of unactivated homobenzylic halides.
    Saito B, Fu GC.
    J Am Chem Soc; 2008 May 28; 130(21):6694-5. PubMed ID: 18447357
    [Abstract] [Full Text] [Related]

  • 15. Enantioselective alkenylation via nickel-catalyzed cross-coupling with organozirconium reagents.
    Lou S, Fu GC.
    J Am Chem Soc; 2010 Apr 14; 132(14):5010-1. PubMed ID: 20302338
    [Abstract] [Full Text] [Related]

  • 16. Enantioselective Csp3-Csp3 formation by nickel-catalyzed enantioconvergent cross-electrophile alkyl-alkyl coupling of unactivated alkyl halides.
    Zhao WT, Shu W.
    Sci Adv; 2023 Jul 07; 9(27):eadg9898. PubMed ID: 37418514
    [Abstract] [Full Text] [Related]

  • 17. Catalytic enantioselective cyclization/cross-coupling with alkyl electrophiles.
    Cong H, Fu GC.
    J Am Chem Soc; 2014 Mar 12; 136(10):3788-91. PubMed ID: 24575754
    [Abstract] [Full Text] [Related]

  • 18. Silicon-Carbon Bond Formation via Nickel-Catalyzed Cross-Coupling of Silicon Nucleophiles with Unactivated Secondary and Tertiary Alkyl Electrophiles.
    Chu CK, Liang Y, Fu GC.
    J Am Chem Soc; 2016 May 25; 138(20):6404-7. PubMed ID: 27187869
    [Abstract] [Full Text] [Related]

  • 19. Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides.
    Lu Z, Wilsily A, Fu GC.
    J Am Chem Soc; 2011 Jun 01; 133(21):8154-7. PubMed ID: 21553917
    [Abstract] [Full Text] [Related]

  • 20. Catalyst-controlled doubly enantioconvergent coupling of racemic alkyl nucleophiles and electrophiles.
    Huo H, Gorsline BJ, Fu GC.
    Science; 2020 Jan 31; 367(6477):559-564. PubMed ID: 32001652
    [Abstract] [Full Text] [Related]

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