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Journal Abstract Search

291 related items for PubMed ID: 26883465

  • 1.
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  • 2. Synthesis of spiro-tetrahydrothiopyran-oxindoles by Michael-aldol cascade reactions: discovery of potential P53-MDM2 inhibitors with good antitumor activity.
    Wang S, Chen S, Guo Z, He S, Zhang F, Liu X, Chen W, Zhang S, Sheng C.
    Org Biomol Chem; 2018 Jan 24; 16(4):625-634. PubMed ID: 29302672
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  • 5. Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction.
    Ding K, Lu Y, Nikolovska-Coleska Z, Wang G, Qiu S, Shangary S, Gao W, Qin D, Stuckey J, Krajewski K, Roller PP, Wang S.
    J Med Chem; 2006 Jun 15; 49(12):3432-5. PubMed ID: 16759082
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  • 7. Organocatalytic Asymmetric Michael/Friedel-Crafts Cascade Reaction of 3-Pyrrolyl-oxindoles and α,β-Unsaturated Aldehydes for the Construction of Chiral Spiro[5,6-dihydropyrido[1,2-a]pyrrole-3,3'-oxindoles].
    You Y, Cui BD, Zhou MQ, Zuo J, Zhao JQ, Xu XY, Zhang XM, Yuan WC.
    J Org Chem; 2015 Jun 05; 80(11):5951-7. PubMed ID: 25984596
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  • 8. Catalytic asymmetric construction of 3,3'-spirooxindoles fused with seven-membered rings by enantioselective tandem reactions.
    Wang Y, Shi F, Yao XX, Sun M, Dong L, Tu SJ.
    Chemistry; 2014 Nov 10; 20(46):15047-52. PubMed ID: 25255976
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  • 9. Highly diastereo- and enantioselective construction of a spiro[cyclopenta[b]indole-1,3'-oxindole] scaffold via catalytic asymmetric formal [3+2] cycloadditions.
    Tan W, Li X, Gong YX, Ge MD, Shi F.
    Chem Commun (Camb); 2014 Dec 28; 50(100):15901-4. PubMed ID: 25380514
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  • 11. An organocatalytic Michael-Michael cascade for the enantioselective construction of spirocyclopentane bioxindoles: control of four contiguous stereocenters.
    Sun W, Hong L, Zhu G, Wang Z, Wei X, Ni J, Wang R.
    Org Lett; 2014 Jan 17; 16(2):544-7. PubMed ID: 24400909
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  • 12. Diastereo- and enantioselective construction of a bispirooxindole scaffold containing a tetrahydro-β-carboline moiety through an organocatalytic asymmetric cascade reaction.
    Dai W, Lu H, Li X, Shi F, Tu SJ.
    Chemistry; 2014 Sep 01; 20(36):11382-9. PubMed ID: 25056997
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  • 13. Spiro-oxindole derivative 5-chloro-4',5'-diphenyl-3'-(4-(2-(piperidin-1-yl) ethoxy) benzoyl) spiro[indoline-3,2'-pyrrolidin]-2-one triggers apoptosis in breast cancer cells via restoration of p53 function.
    Saxena R, Gupta G, Manohar M, Debnath U, Popli P, Prabhakar YS, Konwar R, Kumar S, Kumar A, Dwivedi A.
    Int J Biochem Cell Biol; 2016 Jan 01; 70():105-17. PubMed ID: 26556313
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  • 14. Diastereo- and Enantioselective Construction of 3,3'-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions.
    Dai W, Jiang XL, Wu Q, Shi F, Tu SJ.
    J Org Chem; 2015 Jun 05; 80(11):5737-44. PubMed ID: 25939045
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  • 19. Organocatalytic enantioselective construction of multi-functionalized spiro oxindole dienes.
    Huang XF, Zhang YF, Qi ZH, Li NK, Geng ZC, Li K, Wang XW.
    Org Biomol Chem; 2014 Jul 07; 12(25):4372-85. PubMed ID: 24840651
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  • 20. Enantioselective synthesis of substituted oxindoles and spirooxindoles with applications in drug discovery.
    Badillo JJ, Hanhan NV, Franz AK.
    Curr Opin Drug Discov Devel; 2010 Jul 07; 13(6):758-76. PubMed ID: 21061236
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