BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 23435435)

  • 1. A highly enantioselective four-component reaction for the efficient construction of chiral β-hydroxy-α-amino acid derivatives.
    Qian Y; Jing C; Liu S; Hu W
    Chem Commun (Camb); 2013 Apr; 49(26):2700-2. PubMed ID: 23435435
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Catalytic enantioselective aldol additions of alpha-isothiocyanato imides to alpha-ketoesters.
    Vecchione MK; Li L; Seidel D
    Chem Commun (Camb); 2010 Jul; 46(25):4604-6. PubMed ID: 20485801
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An easy approach to optically active alpha-amino phosphonic acid derivatives by chiral Zn(II)-catalyzed enantioselective amination of phosphonates.
    Bernardi L; Zhuang W; Jørgensen KA
    J Am Chem Soc; 2005 Apr; 127(16):5772-3. PubMed ID: 15839659
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Catalytic asymmetric addition of beta-keto phosphonates to an activated imine--formation of optically active functionalized phosphonate alpha-amino acid derivatives.
    Kjaersgaard A; Jørgensen KA
    Org Biomol Chem; 2005 Mar; 3(5):804-8. PubMed ID: 15731866
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lewis acid promoted highly diastereoselective Petasis Borono-Mannich reaction: efficient synthesis of optically active β,γ-unsaturated α-amino acids.
    Li Y; Xu MH
    Org Lett; 2012 Apr; 14(8):2062-5. PubMed ID: 22480132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aniline mediated oxidative C-C bond cleavage of α-alkoxy aldehydes in air and a model reaction for the synthesis of α-(D)-amino acid derivatives.
    Hu B; Li Y; Li Z; Meng X
    Org Biomol Chem; 2013 Jul; 11(25):4138-41. PubMed ID: 23712772
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A highly enantioselective route to either enantiomer of both alpha- and beta-amino acid derivatives.
    Córdova A; Watanabe S; Tanaka F; Notz W; Barbas CF
    J Am Chem Soc; 2002 Mar; 124(9):1866-7. PubMed ID: 11866595
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diastereoselective conjugate addition to chiral alpha,beta-unsaturated carbonyl systems in aqueous media: an enantioselective entry to alpha- and gamma-hydroxy acids and alpha-amino acids.
    Suárez RM; Pérez Sestelo J; Sarandeses LA
    Chemistry; 2003 Sep; 9(17):4179-87. PubMed ID: 12953203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A highly diastereoselective synthesis of α-hydroxy-β-amino acid derivatives via a Lewis acid catalyzed three-component condensation reaction.
    Gassa F; Contini A; Fontana G; Pellegrino S; Gelmi ML
    J Org Chem; 2010 Nov; 75(21):7099-106. PubMed ID: 20945864
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Highly diastereo- and enantioselective reactions of enecarbamates with ethyl glyoxylate to give optically active syn and anti alpha-alkyl-beta-hydroxy imines and ketones.
    Matsubara R; Nakamura Y; Kobayashi S
    Angew Chem Int Ed Engl; 2004 Jun; 43(25):3258-60. PubMed ID: 15213948
    [No Abstract]   [Full Text] [Related]  

  • 11. Direct organocatalytic asymmetric aldol reactions of alpha-amino aldehydes: expedient syntheses of highly enantiomerically enriched anti-beta-hydroxy-alpha-amino acids.
    Thayumanavan R; Tanaka F; Barbas III CF
    Org Lett; 2004 Sep; 6(20):3541-4. PubMed ID: 15387543
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Catalytic enantioselective addition of propionate units to imines: an efficient synthesis of anti-alpha-methyl-beta-amino acid derivatives.
    Kobayashi S; Kobayashi J; Ishitani H; Ueno M
    Chemistry; 2002 Sep; 8(18):4185-90. PubMed ID: 12298008
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copper-catalyzed asymmetric hydroboration of α-dehydroamino acid derivatives: facile synthesis of chiral β-hydroxy-α-amino acids.
    He ZT; Zhao YS; Tian P; Wang CC; Dong HQ; Lin GQ
    Org Lett; 2014 Mar; 16(5):1426-9. PubMed ID: 24528372
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Highly efficient synthesis of mixed 3,3'-bisindoles via Rh(II)-catalyzed three-component reaction of 3-diazooxindoles with indoles and ethyl glyoxylate.
    Xing D; Jing C; Li X; Qiu H; Hu W
    Org Lett; 2013 Jul; 15(14):3578-81. PubMed ID: 23808602
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Asymmetric transfer hydrogenation coupled with dynamic kinetic resolution in water: synthesis of anti-β-hydroxy-α-amino acid derivatives.
    Seashore-Ludlow B; Saint-Dizier F; Somfai P
    Org Lett; 2012 Dec; 14(24):6334-7. PubMed ID: 23227944
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enantioselective synthesis of cyclic quaternary α-amino acid derivatives by chiral phosphoric acid catalysis.
    Wang L; Rahman A; Lin X
    Org Biomol Chem; 2017 Jul; 15(28):6033-6041. PubMed ID: 28681891
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cooperative catalysis with chiral Brønsted acid-Rh2(OAc)4: highly enantioselective three-component reactions of diazo compounds with alcohols and imines.
    Hu W; Xu X; Zhou J; Liu WJ; Huang H; Hu J; Yang L; Gong LZ
    J Am Chem Soc; 2008 Jun; 130(25):7782-3. PubMed ID: 18512907
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rhodium-catalyzed enantioselective 1,2-addition of arylboronic acids to heteroaryl α-ketoesters for synthesis of heteroaromatic α-hydroxy esters.
    Wang H; Zhu TS; Xu MH
    Org Biomol Chem; 2012 Dec; 10(46):9158-64. PubMed ID: 23011218
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Enantioselective organocatalytic synthesis of quaternary α-amino acids bearing a CF3 moiety.
    Husmann R; Sugiono E; Mersmann S; Raabe G; Rueping M; Bolm C
    Org Lett; 2011 Mar; 13(5):1044-7. PubMed ID: 21348534
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A powerful synergistic effect for highly efficient diastereo- and enantioselective phase-transfer catalyzed conjugate additions.
    Hua MQ; Wang L; Cui HF; Nie J; Zhang XL; Ma JA
    Chem Commun (Camb); 2011 Feb; 47(5):1631-3. PubMed ID: 21116533
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.