BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 12916992)

  • 1. beta-Isocupreidine-catalyzed asymmetric Baylis-Hillman reaction of imines.
    Kawahara S; Nakano A; Esumi T; Iwabuchi Y; Hatakeyama S
    Org Lett; 2003 Aug; 5(17):3103-5. PubMed ID: 12916992
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Beta-isocupreidine-catalyzed Baylis-Hillman reaction of chiral N-boc-alpha-amino aldehydes.
    Nakano A; Takahashi K; Ishihara J; Hatakeyama S
    Org Lett; 2006 Nov; 8(23):5357-60. PubMed ID: 17078717
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Invertible enantioselectivity in 6'-deoxy-6'-acylamino-beta-isocupreidine-catalyzed asymmetric aza-Morita-Baylis-Hillman reaction: key role of achiral additive.
    Abermil N; Masson G; Zhu J
    Org Lett; 2009 Oct; 11(20):4648-51. PubMed ID: 19775129
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chiral phosphine lewis bases catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins.
    Shi M; Chen LH; Li CQ
    J Am Chem Soc; 2005 Mar; 127(11):3790-800. PubMed ID: 15771513
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Asymmetric catalytic aza-Morita-Baylis-Hillman reaction (aza-MBH): an interesting functional group-caused reversal of asymmetric induction.
    Shi M; Qi MJ; Liu XG
    Chem Commun (Camb); 2008 Dec; (45):6025-7. PubMed ID: 19030574
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Highly enantioselective aza Morita-Baylis-Hillman reaction catalyzed by bifunctional beta-isocupreidine derivatives.
    Abermil N; Masson G; Zhu J
    J Am Chem Soc; 2008 Sep; 130(38):12596-7. PubMed ID: 18729367
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Catalytic, asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins by quinidine-derived chiral amines.
    Shi M; Xu YM; Shi YL
    Chemistry; 2005 Mar; 11(6):1794-802. PubMed ID: 15669042
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Highly efficient aza-Baylis-Hillman reaction of N-tosylated imines with MVK, acrolein, and phenyl acrylate or alpha-naphthyl acrylate: Lewis base effects and a convenient method to synthesize alpha,beta-unsaturated beta-amino carbonyl compounds.
    Xu YM; Shi M
    J Org Chem; 2004 Jan; 69(2):417-25. PubMed ID: 14725455
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Enantioselective synthesis of the optically active alpha-methylene-beta-hydroxy esters, equivalent compounds to Morita-Baylis-Hillman adducts, using successive asymmetric aldol reaction and oxidative deselenization.
    Shiina I; Yamai YS; Shimazaki T
    J Org Chem; 2005 Sep; 70(20):8103-6. PubMed ID: 16277334
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Baylis-Hillman reactions of N-tosyl aldimines and aryl aldehydes with 3-methylpenta-3,4-dien-2-one.
    Zhao GL; Shi M
    Org Biomol Chem; 2005 Oct; 3(20):3686-94. PubMed ID: 16211103
    [TBL] [Abstract][Full Text] [Related]  

  • 11. N-carbamate protected alpha-amidoalkyl-p-tolylsulfones: convenient substrates in the aza-Morita-Baylis-Hillman reaction.
    Gajda A; Gajda T
    J Org Chem; 2008 Nov; 73(21):8643-6. PubMed ID: 18821802
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dual catalyst control in the amino acid-peptide-catalyzed enantioselective Baylis-Hillman reaction.
    Imbriglio JE; Vasbinder MM; Miller SJ
    Org Lett; 2003 Oct; 5(20):3741-3. PubMed ID: 14507219
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Abnormal aza-Baylis-Hillman reaction of N-tosylated imines with ethyl 2,3-butadienoate and penta-3,4-dien-2-one.
    Zhao GL; Huang JW; Shi M
    Org Lett; 2003 Nov; 5(24):4737-9. PubMed ID: 14627428
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Asymmetric synthesis of 2-alkyl-substituted 2,5-dihydropyrroles from optically active aza-Baylis-Hillman adducts. Formal synthesis of (-)-trachelanthamidine.
    Ishikawa S; Noguchi F; Kamimura A
    J Org Chem; 2010 Jun; 75(11):3578-86. PubMed ID: 20465267
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Asymmetric Baylis-Hillman reactions promoted by chiral imidazolines.
    Xu J; Guan Y; Yang S; Ng Y; Peh G; Tan CH
    Chem Asian J; 2006 Nov; 1(5):724-9. PubMed ID: 17441115
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Asymmetric Mannich reactions with in situ generation of carbamate-protected imines by an organic catalyst.
    Song J; Shih HW; Deng L
    Org Lett; 2007 Feb; 9(4):603-6. PubMed ID: 17256945
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chiral Lewis acid-catalyzed asymmetric Baylis-Hillman reactions.
    Yang KS; Lee WD; Pan JF; Chen K
    J Org Chem; 2003 Feb; 68(3):915-9. PubMed ID: 12558416
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First asymmetric synthesis of chiral beta-iodo Baylis-Hillman esters via tandem 1,4-conjugate addition/carbonyl coupling reactions.
    Xu X; Chen D; Wei HX; Li G; Xiao TL; Armstrong DW
    Chirality; 2003 Feb; 15(2):139-42. PubMed ID: 12520505
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Asymmetric thio-Michael/nucleophilic addition domino reaction with chiral N-sulfinimines.
    Kamimura A; Okawa H; Morisaki Y; Ishikawa S; Uno H
    J Org Chem; 2007 Apr; 72(9):3569-72. PubMed ID: 17407353
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Practical Proline-catalyzed asymmetric Mannich reaction of aldehydes with N-Boc-imines.
    Yang JW; Stadler M; List B
    Nat Protoc; 2007; 2(8):1937-42. PubMed ID: 17703205
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.