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PUBMED FOR HANDHELDS

Journal Abstract Search


372 related items for PubMed ID: 18447357

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  • 2. Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides.
    Arp FO, Fu GC.
    J Am Chem Soc; 2005 Aug 03; 127(30):10482-3. PubMed ID: 16045323
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  • 4. Suzuki cross-couplings of unactivated secondary alkyl bromides and iodides.
    Zhou J, Fu GC.
    J Am Chem Soc; 2004 Feb 11; 126(5):1340-1. PubMed ID: 14759182
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  • 7. Asymmetric cross-coupling of non-activated secondary alkyl halides.
    Glorius F.
    Angew Chem Int Ed Engl; 2008 Feb 11; 47(44):8347-9. PubMed ID: 18814168
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  • 8. Methods and Mechanisms for Cross-Electrophile Coupling of Csp(2) Halides with Alkyl Electrophiles.
    Weix DJ.
    Acc Chem Res; 2015 Jun 16; 48(6):1767-75. PubMed ID: 26011466
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  • 13. A nonsymmetric pincer-catalyzed Suzuki-Miyaura arylation of benzyl halides and other nonactivated unusual coupling partners.
    Inés B, Moreno I, SanMartin R, Domínguez E.
    J Org Chem; 2008 Nov 07; 73(21):8448-51. PubMed ID: 18855448
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  • 14. The first applications of carbene ligands in cross-couplings of alkyl electrophiles: sonogashira reactions of unactivated alkyl bromides and iodides.
    Eckhardt M, Fu GC.
    J Am Chem Soc; 2003 Nov 12; 125(45):13642-3. PubMed ID: 14599185
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  • 15. 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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  • 16. Amino alcohols as ligands for nickel-catalyzed suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids.
    González-Bobes F, Fu GC.
    J Am Chem Soc; 2006 Apr 26; 128(16):5360-1. PubMed ID: 16620105
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  • 18. 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
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  • 19. 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
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