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Journal Abstract Search

135 related items for PubMed ID: 35925763

  • 21. Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides.
    Wang Z, Yang ZP, Fu GC.
    Nat Chem; 2021 Mar; 13(3):236-242. PubMed ID: 33432109
    [Abstract] [Full Text] [Related]

  • 22. 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
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  • 26. 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
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  • 29. [Asymmetric synthesis using chiral bases].
    Koga K, Odashima K.
    Yakugaku Zasshi; 1997 Nov 01; 117(10-11):800-16. PubMed ID: 9414592
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  • 30. 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
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  • 32. 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
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  • 33. Catalytic asymmetric synthesis of secondary nitriles via stereoconvergent Negishi arylations and alkenylations of racemic α-bromonitriles.
    Choi J, Fu GC.
    J Am Chem Soc; 2012 Jun 06; 134(22):9102-5. PubMed ID: 22612264
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  • 37. 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
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  • 38. Nickel-Catalyzed Radical Mechanisms: Informing Cross-Coupling for Synthesizing Non-Canonical Biomolecules.
    Dawson GA, Spielvogel EH, Diao T.
    Acc Chem Res; 2023 Dec 19; 56(24):3640-3653. PubMed ID: 38033206
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  • 39. Asymmetric Suzuki cross-couplings of activated secondary alkyl electrophiles: arylations of racemic alpha-chloroamides.
    Lundin PM, Fu GC.
    J Am Chem Soc; 2010 Aug 18; 132(32):11027-9. PubMed ID: 20698665
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  • 40. Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.
    Behenna DC, Mohr JT, Sherden NH, Marinescu SC, Harned AM, Tani K, Seto M, Ma S, Novák Z, Krout MR, McFadden RM, Roizen JL, Enquist JA, White DE, Levine SR, Petrova KV, Iwashita A, Virgil SC, Stoltz BM.
    Chemistry; 2011 Dec 09; 17(50):14199-223. PubMed ID: 22083969
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