BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

303 related articles for article (PubMed ID: 26295594)

  • 1. A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
    Ding R; Zheng B; Wang Y; Peng Y
    Org Lett; 2015 Sep; 17(17):4128-31. PubMed ID: 26295594
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Organocatalytic Synthesis of Highly Functionalized Heterocycles by Enantioselective aza-Morita-Baylis-Hillman-Type Domino Reactions.
    Takizawa S
    Chem Pharm Bull (Tokyo); 2020; 68(4):299-315. PubMed ID: 32238648
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Squaramide-catalyzed enantioselective Michael addition of malononitrile to chalcones.
    Yang W; Jia Y; Du DM
    Org Biomol Chem; 2012 Jan; 10(2):332-8. PubMed ID: 22071519
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Asymmetric catalytic aza-Morita-Baylis-Hillman reaction for the synthesis of 3-substituted-3-aminooxindoles with chiral quaternary carbon centers.
    Hu FL; Wei Y; Shi M; Pindi S; Li G
    Org Biomol Chem; 2013 Mar; 11(12):1921-4. PubMed ID: 23407608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An enantioselective organocatalyzed aza-Morita-Baylis-Hillman reaction of isatin-derived ketimines with acrolein.
    Yoshida Y; Sako M; Kishi K; Sasai H; Hatakeyama S; Takizawa S
    Org Biomol Chem; 2015 Sep; 13(34):9022-8. PubMed ID: 26214279
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Organocatalytic Enantioselective [1 + 4] Annulation of Morita-Baylis-Hillman Carbonates with Electron-Deficient Olefins: Access to Chiral 2,3-Dihydrofuran Derivatives.
    Cheng Y; Han Y; Li P
    Org Lett; 2017 Sep; 19(18):4774-4777. PubMed ID: 28846432
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diversity-oriented asymmetric catalysis (DOAC): stereochemically divergent synthesis of thiochromanes using an imidazoline-aminophenol-nickel-catalyzed Michael/Henry reaction.
    Arai T; Yamamoto Y
    Org Lett; 2014 Mar; 16(6):1700-3. PubMed ID: 24601640
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enantioselective aza-Morita-Baylis-Hillman reaction between acrylates and N-Boc isatin ketimines: asymmetric construction of chiral 3-substituted-3-aminooxindoles.
    Zhao X; Li TZ; Qian JY; Sha F; Wu XY
    Org Biomol Chem; 2014 Oct; 12(40):8072-8. PubMed ID: 25184554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Efficient direct asymmetric vinylogous Michael addition reactions of gamma-butenolides to chalcones catalyzed by vicinal primary-diamine salts.
    Wang J; Qi C; Ge Z; Cheng T; Li R
    Chem Commun (Camb); 2010 Mar; 46(12):2124-6. PubMed ID: 20221513
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A chiral benzoylthiourea-pyrrolidine catalyst for the highly enantioselective Michael addition of ketones to chalcones.
    Ban SR; Zhu XX; Zhang ZP; Li QS
    Bioorg Med Chem Lett; 2014 Jun; 24(11):2517-20. PubMed ID: 24755429
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Organocatalytic asymmetric domino aza-Michael-Mannich reaction: synthesis of tetrahydroimidazopyrimidine derivatives.
    Li H; Zhao J; Zeng L; Hu W
    J Org Chem; 2011 Oct; 76(19):8064-9. PubMed ID: 21830809
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chiral bisguanidine-catalyzed inverse-electron-demand hetero-Diels-Alder reaction of chalcones with azlactones.
    Dong S; Liu X; Chen X; Mei F; Zhang Y; Gao B; Lin L; Feng X
    J Am Chem Soc; 2010 Aug; 132(31):10650-1. PubMed ID: 20681686
    [TBL] [Abstract][Full Text] [Related]  

  • 15. New multifunctional chiral phosphines and BINOL derivatives co-catalyzed enantioselective aza-Morita-Baylis-Hillman reaction of 5,5-disubstituted cyclopent-2-enone and N-sulfonated imines.
    Yang YL; Wei Y; Shi M
    Org Biomol Chem; 2012 Sep; 10(36):7429-38. PubMed ID: 22885992
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Asymmetric synthesis of α,β-diamino acid derivatives with an aziridine-, azetidine- and γ-lactone-skeleton via Mannich-type additions across α-chloro-N-sulfinylimines.
    Callebaut G; Mangelinckx S; Kiss L; Sillanpää R; Fülöp F; De Kimpe N
    Org Biomol Chem; 2012 Mar; 10(11):2326-38. PubMed ID: 22311107
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines.
    Lin GQ; Xu MH; Zhong YW; Sun XW
    Acc Chem Res; 2008 Jul; 41(7):831-40. PubMed ID: 18533688
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ruthenium(II)/chiral Brønsted acid co-catalyzed enantioselective four-component reaction/cascade aza-Michael addition for efficient construction of 1,3,4-tetrasubstituted tetrahydroisoquinolines.
    Jiang J; Ma X; Ji C; Guo Z; Shi T; Liu S; Hu W
    Chemistry; 2014 Feb; 20(6):1505-9. PubMed ID: 24436086
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chiral brønsted Acid-catalyzed stereoselective Mannich-type reaction of azlactones with aldimines.
    Ávila EP; Justo RM; Gonçalves VP; Pereira AA; Diniz R; Amarante GW
    J Org Chem; 2015 Jan; 80(1):590-4. PubMed ID: 25469764
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Organocatalytic enantioselective decarboxylative reaction of malonic acid half thioesters with cyclic N-sulfonyl ketimines by using N-heteroarenesulfonyl cinchona alkaloid amides.
    Nakamura S; Sano M; Toda A; Nakane D; Masuda H
    Chemistry; 2015 Mar; 21(10):3929-32. PubMed ID: 25614368
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.