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141 related items for PubMed ID: 38061195

  • 1. Catalytic Asymmetric α-Alkylation of Ketones with Unactivated Alkyl Halides.
    Wang P, Zhu L, Wang J, Tao Z.
    J Am Chem Soc; 2023 Dec 20; 145(50):27211-27217. PubMed ID: 38061195
    [Abstract] [Full Text] [Related]

  • 2. Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks.
    Kwiatkowski MR, Alexanian EJ.
    Acc Chem Res; 2019 Apr 16; 52(4):1134-1144. PubMed ID: 30908013
    [Abstract] [Full Text] [Related]

  • 3. Enantioselective alkylations of tributyltin enolates catalyzed by Cr(salen)Cl: access to enantiomerically enriched all-carbon quaternary centers.
    Doyle AG, Jacobsen EN.
    J Am Chem Soc; 2005 Jan 12; 127(1):62-3. PubMed ID: 15631449
    [Abstract] [Full Text] [Related]

  • 4. Enantioselective C(sp3)-C(sp3) Reductive Cross-Electrophile Coupling of Unactivated Alkyl Halides with α-Chloroboronates via Dual Nickel/Photoredox Catalysis.
    Zhou J, Wang D, Xu W, Hu Z, Xu T.
    J Am Chem Soc; 2023 Feb 01; 145(4):2081-2087. PubMed ID: 36688920
    [Abstract] [Full Text] [Related]

  • 5. Asymmetric construction of acyclic quaternary stereocenters via direct enantioselective additions of α-alkynyl ketones to allenamides.
    Wang J, He F, Yang X.
    Nat Commun; 2021 Nov 18; 12(1):6700. PubMed ID: 34795297
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Highly enantioselective phase-transfer-catalyzed alkylation of protected alpha-amino acid amides toward practical asymmetric synthesis of vicinal diamines, alpha-amino ketones, and alpha-amino alcohols.
    Ooi T, Takeuchi M, Kato D, Uematsu Y, Tayama E, Sakai D, Maruoka K.
    J Am Chem Soc; 2005 Apr 13; 127(14):5073-83. PubMed ID: 15810842
    [Abstract] [Full Text] [Related]

  • 8. Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).
    Terao J, Kambe N.
    Acc Chem Res; 2008 Nov 18; 41(11):1545-54. PubMed ID: 18973349
    [Abstract] [Full Text] [Related]

  • 9. 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 18; 48(56):7034-6. PubMed ID: 22684052
    [Abstract] [Full Text] [Related]

  • 10. Catalytic Asymmetric Barbier Reaction of Ketones with Unactivated Alkyl Electrophiles.
    Xia H, Jiang X, Lin D, Zhang S, Yu Z, Wu X, Qu J, Chen Y.
    J Am Chem Soc; 2024 Oct 03. PubMed ID: 39361011
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Direct Acylation of Unactivated Alkyl Halides with Aldehydes through N-Heterocyclic Carbene Organocatalysis.
    Li QZ, Zeng R, Xu PS, Jin XH, Xie C, Yang QC, Zhang X, Li JL.
    Angew Chem Int Ed Engl; 2023 Oct 02; 62(40):e202309572. PubMed ID: 37581950
    [Abstract] [Full Text] [Related]

  • 13. Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings.
    Zultanski SL, Fu GC.
    J Am Chem Soc; 2011 Oct 05; 133(39):15362-4. PubMed ID: 21913638
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 14(12):3044-7. PubMed ID: 22651806
    [Abstract] [Full Text] [Related]

  • 15. Formal enantioconvergent substitution of alkyl halides via catalytic asymmetric photoredox radical coupling.
    Li J, Kong M, Qiao B, Lee R, Zhao X, Jiang Z.
    Nat Commun; 2018 Jun 22; 9(1):2445. PubMed ID: 29934495
    [Abstract] [Full Text] [Related]

  • 16. Synergistic Merger of Ketone, Halogen Atom Transfer (XAT), and Nickel-Mediated C(sp3)-C(sp2) Cross-Electrophile Coupling Enabled by Light.
    Tripathy AR, Bisoyi A, P A, Venugopal S, Yatham VR.
    ACS Org Inorg Au; 2024 Apr 03; 4(2):229-234. PubMed ID: 38585508
    [Abstract] [Full Text] [Related]

  • 17. Nickel-Catalyzed Asymmetric Addition of Aromatic Halides to Ketones: Highly Enantioselective Synthesis of Chiral 2,3-Dihydrobenzofurans Containing a Tertiary Alcohol.
    Li Y, Li W, Tian J, Huang G, Lv H.
    Org Lett; 2020 Jul 17; 22(14):5353-5357. PubMed ID: 32573236
    [Abstract] [Full Text] [Related]

  • 18. Visible-Light-Driven Palladium-Catalyzed Radical Alkylation of C-H Bonds with Unactivated Alkyl Bromides.
    Zhou WJ, Cao GM, Shen G, Zhu XY, Gui YY, Ye JH, Sun L, Liao LL, Li J, Yu DG.
    Angew Chem Int Ed Engl; 2017 Dec 04; 56(49):15683-15687. PubMed ID: 29048716
    [Abstract] [Full Text] [Related]

  • 19. Nickel-Catalyzed Defluorinative Reductive Cross-Coupling of gem-Difluoroalkenes with Unactivated Secondary and Tertiary Alkyl Halides.
    Lu X, Wang Y, Zhang B, Pi JJ, Wang XX, Gong TJ, Xiao B, Fu Y.
    J Am Chem Soc; 2017 Sep 13; 139(36):12632-12637. PubMed ID: 28849923
    [Abstract] [Full Text] [Related]

  • 20. Nickel-Catalyzed Ligand-Controlled Selective Reductive Cyclization/Cross-Couplings.
    Pan Q, Ping Y, Kong W.
    Acc Chem Res; 2023 Mar 07; 56(5):515-535. PubMed ID: 36688822
    [Abstract] [Full Text] [Related]

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