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Journal Abstract Search

571 related items for PubMed ID: 23919290

  • 21. β-C(sp(3))-H Arylation of α-Hydroxy Acid Derivatives Utilizing Amino Acid as a Directing Group.
    Toba T, Hu Y, Tran AT, Yu JQ.
    Org Lett; 2015 Dec 18; 17(24):5966-9. PubMed ID: 26635188
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  • 22. Catalytic intermolecular allylic C-H alkylation.
    Young AJ, White MC.
    J Am Chem Soc; 2008 Oct 29; 130(43):14090-1. PubMed ID: 18831588
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  • 25. 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
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  • 26. Highly stereoselective modifications of peptides via Pd-catalyzed allylic alkylation of internal peptide amide enolates.
    Datta S, Bayer A, Kazmaier U.
    Org Biomol Chem; 2012 Oct 03; 10(41):8268-75. PubMed ID: 22986919
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  • 27. Stereoselective and Site-Specific Allylic Alkylation of Amino Acids and Small Peptides via a Pd/Cu Dual Catalysis.
    Huo X, He R, Fu J, Zhang J, Yang G, Zhang W.
    J Am Chem Soc; 2017 Jul 26; 139(29):9819-9822. PubMed ID: 28686426
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  • 32. Selective peptide modifications via ruthenium-catalyzed allylic alkylations.
    Bayer A, Kazmaier U.
    J Org Chem; 2014 Sep 05; 79(17):8491-7. PubMed ID: 25118961
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  • 33. Nickel-catalyzed chelation-assisted direct arylation of unactivated C(sp3)-H bonds with aryl halides.
    Li M, Dong J, Huang X, Li K, Wu Q, Song F, You J.
    Chem Commun (Camb); 2014 Apr 18; 50(30):3944-6. PubMed ID: 24599346
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  • 39. Catalytic functionalization of unactivated sp3 C-H bonds via exo-directing groups: synthesis of chemically differentiated 1,2-diols.
    Ren Z, Mo F, Dong G.
    J Am Chem Soc; 2012 Oct 17; 134(41):16991-4. PubMed ID: 23030547
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  • 40. Palladium(0)/PAr3 -Catalyzed Intermolecular Amination of C(sp(3) )H Bonds: Synthesis of β-Amino Acids.
    He J, Shigenari T, Yu JQ.
    Angew Chem Int Ed Engl; 2015 May 26; 54(22):6545-9. PubMed ID: 25873526
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