BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 23229090)

  • 1. Organocatalytic asymmetric Michael reaction with acylsilane donors.
    Wu L; Li G; Fu Q; Yu L; Tang Z
    Org Biomol Chem; 2013 Jan; 11(3):443-7. PubMed ID: 23229090
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enantioselective synthesis of optically active cis-β-thio-α-amino acid derivatives through an organocatalytic cascade thio-Michael/ring opening process.
    Geng ZC; Li N; Chen J; Huang XF; Wu B; Liu GG; Wang XW
    Chem Commun (Camb); 2012 May; 48(39):4713-5. PubMed ID: 22473305
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dynamic kinetic resolution in the asymmetric synthesis of beta-amino acids by organocatalytic reduction of enamines with trichlorosilane.
    Malkov AV; Stoncius S; Vranková K; Arndt M; Kocovský P
    Chemistry; 2008; 14(27):8082-5. PubMed ID: 18666274
    [No Abstract]   [Full Text] [Related]  

  • 4. Catalyst control in sequential asymmetric allylic substitution: stereodivergent access to N,N-diprotected unnatural amino acids.
    Tosatti P; Campbell AJ; House D; Nelson A; Marsden SP
    J Org Chem; 2011 Jul; 76(13):5495-501. PubMed ID: 21563816
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Catalytic enantioselective silylation of N-sulfonylimines: asymmetric synthesis of α-amino acids from CO2 via stereospecific carboxylation of α-amino silanes.
    Mita T; Sugawara M; Saito K; Sato Y
    Org Lett; 2014 Jun; 16(11):3028-31. PubMed ID: 24834796
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combinatorial design of simplified high-performance chiral phase-transfer catalysts for practical asymmetric synthesis of alpha-alkyl- and alpha,alpha-dialkyl-alpha-amino acids.
    Kitamura M; Shirakawa S; Arimura Y; Wang X; Maruoka K
    Chem Asian J; 2008 Sep; 3(8-9):1702-14. PubMed ID: 18683160
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis of a series of novel chiral Lewis base catalysts and their application in promoting asymmetric hydrosilylation of β-enamino esters.
    Chen X; Hu XY; Shu C; Zhang YH; Zheng YS; Jiang Y; Yuan WC; Liu B; Zhang XM
    Org Biomol Chem; 2013 May; 11(19):3089-93. PubMed ID: 23563603
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Development of a recyclable fluorous chiral phase-transfer catalyst: application to the catalytic asymmetric synthesis of alpha-amino acids.
    Shirakawa S; Tanaka Y; Maruoka K
    Org Lett; 2004 Apr; 6(9):1429-31. PubMed ID: 15101759
    [TBL] [Abstract][Full Text] [Related]  

  • 9. One-pot asymmetric synthesis of seven-membered carbocycles cyclohepta[b]indoles via a sequential organocatalytic Michael/double Friedel-Crafts alkylation reaction.
    Dange NS; Hong BC; Lee CC; Lee GH
    Org Lett; 2013 Aug; 15(15):3914-7. PubMed ID: 23848568
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enantioselective Michael reactions of beta, beta-disubstituted nitroalkenes: a new approach to beta(2,2)-amino acids with hetero-quaternary stereocenters.
    Lu HH; Zhang FG; Meng XG; Duan SW; Xiao WJ
    Org Lett; 2009 Sep; 11(17):3946-9. PubMed ID: 19653671
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Absolute asymmetric synthesis of tertiary α-amino acids.
    Mai TT; Branca M; Gori D; Guillot R; Kouklovsky C; Alezra V
    Angew Chem Int Ed Engl; 2012 May; 51(20):4981-4. PubMed ID: 22488881
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A facile Cu(I)/TF-BiphamPhos-catalyzed asymmetric approach to unnatural α-amino acid derivatives containing gem-bisphosphonates.
    Xue ZY; Li QH; Tao HY; Wang CJ
    J Am Chem Soc; 2011 Aug; 133(30):11757-65. PubMed ID: 21707068
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Guanidine organocatalyst for the asymmetric Mannich-type reaction between α-isothiocyanato imide and sulfonyl imines.
    Chen X; Dong S; Qiao Z; Zhu Y; Xie M; Lin L; Liu X; Feng X
    Chemistry; 2011 Feb; 17(9):2583-6. PubMed ID: 21271617
    [No Abstract]   [Full Text] [Related]  

  • 14. An asymmetric Michael addition of α,α-disubstituted aldehydes to maleimides leading to a one-pot enantioselective synthesis of lactones catalyzed by amino acids.
    Kokotos CG
    Org Lett; 2013 May; 15(10):2406-9. PubMed ID: 23627257
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Asymmetric synthesis of sterically and electronically demanding linear ω-trifluoromethyl containing amino acids via alkylation of chiral equivalents of nucleophilic glycine and alanine.
    Wang J; Lin D; Zhou S; Ding X; Soloshonok VA; Liu H
    J Org Chem; 2011 Jan; 76(2):684-7. PubMed ID: 21182272
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Silicon-based Lewis acid assisted cinchona alkaloid catalysis: highly enantioselective aza-Michael reaction under solvent-free conditions.
    Yang HM; Li L; Li F; Jiang KZ; Shang JY; Lai GQ; Xu LW
    Org Lett; 2011 Dec; 13(24):6508-11. PubMed ID: 22087568
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Asymmetric synthesis of α-methyl-α-amino acids via diastereoselective alkylation of (1S)-(+)-3-carene derived tricyclic iminolactone.
    Lu TJ; Lin CK
    J Org Chem; 2011 Mar; 76(6):1621-33. PubMed ID: 21306163
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Catalytic synthesis of beta3-amino acid derivatives from alpha-amino acids.
    Byrne CM; Church TL; Kramer JW; Coates GW
    Angew Chem Int Ed Engl; 2008; 47(21):3979-83. PubMed ID: 18404750
    [No Abstract]   [Full Text] [Related]  

  • 19. Organocatalytic Michael addition of aldehydes to vinyl sulfones: enantioselective alpha-alkylations of aldehydes and their derivatives.
    Zhu Q; Lu Y
    Org Lett; 2008 Nov; 10(21):4803-6. PubMed ID: 18834133
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Towards organo-click chemistry: development of organocatalytic multicomponent reactions through combinations of aldol, Wittig, Knoevenagel, Michael, Diels-Alder and Huisgen cycloaddition reactions.
    Ramachary DB; Barbas CF
    Chemistry; 2004 Oct; 10(21):5323-31. PubMed ID: 15390208
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.