BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

393 related articles for article (PubMed ID: 22847715)

  • 1. Squaramide-catalysed enantio- and diastereoselective sulfa-Michael addition of thioacetic acid to α,β-disubstituted nitroalkenes.
    Yang W; Du DM
    Org Biomol Chem; 2012 Sep; 10(34):6876-84. PubMed ID: 22847715
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Squaramide-catalysed enantioselective Michael addition of pyrazolin-5-ones to nitroalkenes.
    Li JH; Du DM
    Org Biomol Chem; 2013 Sep; 11(36):6215-23. PubMed ID: 23939139
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Enantioselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea organocatalysis.
    Kimmel KL; Robak MT; Ellman JA
    J Am Chem Soc; 2009 Jul; 131(25):8754-5. PubMed ID: 19496569
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chiral squaramide-catalyzed highly diastereo- and enantioselective direct Michael addition of nitroalkanes to nitroalkenes.
    Yang W; Du DM
    Chem Commun (Camb); 2011 Dec; 47(47):12706-8. PubMed ID: 22042378
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Catalytic asymmetric 1,6-Michael addition of arylthiols to 3-methyl-4-nitro-5-alkenyl-isoxazoles with bifunctional catalysts.
    Pei QL; Sun HW; Wu ZJ; Du XL; Zhang XM; Yuan WC
    J Org Chem; 2011 Oct; 76(19):7849-59. PubMed ID: 21916401
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Direct asymmetric Michael addition of thioether-based aryl sulfanyl-propan-2-one to nitroalkenes catalyzed by a chiral amine-thiourea bifunctional organocatalyst.
    Jiang X; Zhang B; Zhang Y; Lin L; Yan W; Wang R
    Chirality; 2010 Jul; 22(7):625-34. PubMed ID: 20143410
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chiral squaramide-catalysed one-pot enantioselective sulfa-Michael addition/thioesterification of thiols with α,β-unsaturated N-acylated succinimides.
    Zhao BL; Du DM
    Org Biomol Chem; 2014 Mar; 12(10):1585-94. PubMed ID: 24457948
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chiral squaramide-catalyzed asymmetric synthesis of pyranones and pyranonaphthoquinones via cascade reactions of 1,3-dicarbonyls with Morita-Baylis-Hillman acetates of nitroalkenes.
    Nair DK; Menna-Barreto RF; da Silva Júnior EN; Mobin SM; Namboothiri IN
    Chem Commun (Camb); 2014 Jul; 50(53):6973-6. PubMed ID: 24817645
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diastereoselective Michael reaction of chiral nickel(II) glycinate with nitroalkenes for asymmetric synthesis of β-substituted α,γ-diaminobutyric acid derivatives in water.
    Wang J; Ji X; Shi J; Sun H; Jiang H; Liu H
    Amino Acids; 2012 May; 42(5):1685-94. PubMed ID: 21384130
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Squaramide-tertiary amine catalyzed asymmetric cascade sulfa-Michael/Michael addition via dynamic kinetic resolution: access to highly functionalized chromans with three contiguous stereocenters.
    Yang W; Yang Y; Du DM
    Org Lett; 2013 Mar; 15(6):1190-3. PubMed ID: 23463941
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes.
    Zhu Y; Li X; Chen Q; Su J; Jia F; Qiu S; Ma M; Sun Q; Yan W; Wang K; Wang R
    Org Lett; 2015 Aug; 17(15):3826-9. PubMed ID: 26204248
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Organocatalytic highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes.
    Zhou WM; Liu H; Du DM
    Org Lett; 2008 Jul; 10(13):2817-20. PubMed ID: 18533672
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Pyrrolidinyl-camphor derivatives as a new class of organocatalyst for direct asymmetric Michael addition of aldehydes and ketones to beta-nitroalkenes.
    Ting YF; Chang C; Reddy RJ; Magar DR; Chen K
    Chemistry; 2010 Jun; 16(23):7030-8. PubMed ID: 20455225
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Organocatalytic sequential Michael reactions: stereoselective synthesis of multifunctionalized tetrahydroindan derivatives.
    He P; Liu X; Shi J; Lin L; Feng X
    Org Lett; 2011 Mar; 13(5):936-9. PubMed ID: 21309523
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enantioselective organocatalytic oxa-Michael addition of oximes to β-CF3-β-disubstituted nitroalkenes: efficient synthesis of β-amino-α-trifluoromethyl alcohols.
    Liu FL; Chen JR; Feng B; Hu XQ; Ye LH; Lu LQ; Xiao WJ
    Org Biomol Chem; 2014 Feb; 12(7):1057-60. PubMed ID: 24407351
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Asymmetric 1,4-addition of oxazolones to nitroalkenes by bifunctional cinchona alkaloid thiourea organocatalysts: synthesis of alpha,alpha-disubstituted alpha-amino acids.
    Alemán J; Milelli A; Cabrera S; Reyes E; Jørgensen KA
    Chemistry; 2008; 14(35):10958-66. PubMed ID: 18979472
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Highly enantioselective synthesis of nitrocyclopropanes via organocatalytic conjugate addition of bromomalonate to alpha,beta-unsaturated nitroalkenes.
    Xuan YN; Nie SZ; Dong LT; Zhang JM; Yan M
    Org Lett; 2009 Apr; 11(7):1583-6. PubMed ID: 19260703
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins via dienamine catalysis.
    Han B; Xiao YC; He ZQ; Chen YC
    Org Lett; 2009 Oct; 11(20):4660-3. PubMed ID: 19754072
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Proline-based reduced dipeptides as recyclable and highly enantioselective organocatalysts for asymmetric Michael addition.
    Cao X; Wang G; Zhang R; Wei Y; Wang W; Sun H; Chen L
    Org Biomol Chem; 2011 Oct; 9(19):6487-90. PubMed ID: 21829837
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.