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PUBMED FOR HANDHELDS

Journal Abstract Search


189 related items for PubMed ID: 21913638

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. Enantioconvergent cross-couplings of racemic alkylmetal reagents with unactivated secondary alkyl electrophiles: catalytic asymmetric Negishi α-alkylations of N-Boc-pyrrolidine.
    Cordier CJ, Lundgren RJ, Fu GC.
    J Am Chem Soc; 2013 Jul 31; 135(30):10946-9. PubMed ID: 23869442
    [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 17; 134(41):17003-6. PubMed ID: 23039358
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. A nickel catalyst for the addition of organoboronate esters to ketones and aldehydes.
    Bouffard J, Itami K.
    Org Lett; 2009 Oct 01; 11(19):4410-3. PubMed ID: 19708680
    [Abstract] [Full Text] [Related]

  • 8. 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]

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  • 10. Catalytic Enantioselective α-Alkylation of Amides by Unactivated Alkyl Electrophiles.
    Tong X, Schneck F, Fu GC.
    J Am Chem Soc; 2022 Aug 17; 144(32):14856-14863. PubMed ID: 35925763
    [Abstract] [Full Text] [Related]

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  • 12. 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]

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  • 14. Catalytic asymmetric carbon-carbon bond formation via allylic alkylations with organolithium compounds.
    Pérez M, Fañanás-Mastral M, Bos PH, Rudolph A, Harutyunyan SR, Feringa BL.
    Nat Chem; 2011 May 11; 3(5):377-81. PubMed ID: 21505496
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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]

  • 17. 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
    [Abstract] [Full Text] [Related]

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  • 19. Asymmetric intramolecular oxa-Michael addition of activated alpha,beta-unsaturated ketones catalyzed by a chiral N,N'-dioxide nickel(II) complex: highly enantioselective synthesis of flavanones.
    Wang L, Liu X, Dong Z, Fu X, Feng X.
    Angew Chem Int Ed Engl; 2008 Jun 06; 47(45):8670-3. PubMed ID: 18846524
    [No Abstract] [Full Text] [Related]

  • 20. A practical method for enantioselective synthesis of all-carbon quaternary stereogenic centers through NHC-Cu-catalyzed conjugate additions of alkyl- and arylzinc reagents to beta-substituted cyclic enones.
    Lee KS, Brown MK, Hird AW, Hoveyda AH.
    J Am Chem Soc; 2006 Jun 07; 128(22):7182-4. PubMed ID: 16734469
    [Abstract] [Full Text] [Related]


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