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Journal Abstract Search

208 related items for PubMed ID: 22287059

  • 1. Asymmetric synthesis of allenyl oxindoles and spirooxindoles by a catalytic enantioselective Saucy-Marbet Claisen rearrangement.
    Cao T, Deitch J, Linton EC, Kozlowski MC.
    Angew Chem Int Ed Engl; 2012 Mar 05; 51(10):2448-51. PubMed ID: 22287059
    [No Abstract] [Full Text] [Related]

  • 2. Catalytic stereoselective synthesis of diverse oxindoles and spirooxindoles from isatins.
    MacDonald JP, Badillo JJ, Arevalo GE, Silva-García A, Franz AK.
    ACS Comb Sci; 2012 Apr 09; 14(4):285-93. PubMed ID: 22449252
    [Abstract] [Full Text] [Related]

  • 3. Asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles and 3-nitroindoles with amino-thiocarbamate catalysts: enantioselective synthesis of polycyclic spirooxindoles.
    Zhao JQ, Zhou MQ, Wu ZJ, Wang ZH, Yue DF, Xu XY, Zhang XM, Yuan WC.
    Org Lett; 2015 May 01; 17(9):2238-41. PubMed ID: 25875402
    [Abstract] [Full Text] [Related]

  • 4. Copper(II)- and palladium(II)-catalyzed enantioselective Claisen rearrangement of allyloxy- and propargyloxy-indoles to quaternary oxindoles and spirocyclic lactones.
    Cao T, Linton EC, Deitch J, Berritt S, Kozlowski MC.
    J Org Chem; 2012 Dec 21; 77(24):11034-55. PubMed ID: 23167569
    [Abstract] [Full Text] [Related]

  • 5. Zn-Catalyzed Diastereo- and Enantioselective Cascade Reaction of 3-Isothiocyanato Oxindoles and 3-Nitroindoles: Stereocontrolled Syntheses of Polycyclic Spirooxindoles.
    Zhao JQ, Wu ZJ, Zhou MQ, Xu XY, Zhang XM, Yuan WC.
    Org Lett; 2015 Oct 16; 17(20):5020-3. PubMed ID: 26412346
    [Abstract] [Full Text] [Related]

  • 6. Catalytic [4+2] cyclization of α,β-unsaturated acyl chlorides with 3-alkylenyloxindoles: highly diastereo- and enantioselective synthesis of spirocarbocyclic oxindoles.
    Shen LT, Jia WQ, Ye S.
    Angew Chem Int Ed Engl; 2013 Jan 07; 52(2):585-8. PubMed ID: 23150385
    [Abstract] [Full Text] [Related]

  • 7. Enantioselective cascade Michael addition/cyclization reactions of 3-nitro-2H-chromenes with 3-isothiocyanato oxindoles: efficient synthesis of functionalized polycyclic spirooxindoles.
    Tan F, Lu LQ, Yang QQ, Guo W, Bian Q, Chen JR, Xiao WJ.
    Chemistry; 2014 Mar 17; 20(12):3415-20. PubMed ID: 24677230
    [Abstract] [Full Text] [Related]

  • 8. Catalytic asymmetric synthesis of spirooxindoles via addition of isothiocyanato oxindoles to aldehydes under dinuclear nickel Schiff base catalysis.
    Kato S, Kanai M, Matsunaga S.
    Chem Asian J; 2013 Aug 17; 8(8):1768-71. PubMed ID: 23589324
    [No Abstract] [Full Text] [Related]

  • 9. Highly enantioselective construction of spiro[4H-pyran-3,3'-oxindoles] through a domino Knoevenagel/Michael/cyclization sequence catalyzed by cupreine.
    Chen WB, Wu ZJ, Pei QL, Cun LF, Zhang XM, Yuan WC.
    Org Lett; 2010 Jul 16; 12(14):3132-5. PubMed ID: 20545337
    [Abstract] [Full Text] [Related]

  • 10. Catalytic asymmetric Michael addition/cyclization of isothiocyanato oxindoles: highly efficient and versatile approach for the synthesis of 3,2'-pyrrolidinyl mono- and bi-spirooxindole frameworks.
    Cao YM, Shen FF, Zhang FT, Wang R.
    Chemistry; 2013 Jan 21; 19(4):1184-8. PubMed ID: 23255227
    [No Abstract] [Full Text] [Related]

  • 11. An organocatalytic [3+2] cyclisation strategy for the highly enantioselective synthesis of spirooxindoles.
    Voituriez A, Pinto N, Neel M, Retailleau P, Marinetti A.
    Chemistry; 2010 Nov 08; 16(42):12541-4. PubMed ID: 20853298
    [No Abstract] [Full Text] [Related]

  • 12. Scaffold-inspired enantioselective synthesis of biologically important spiro[pyrrolidin-3,2'-oxindoles] with structural diversity through catalytic isatin-derived 1,3-dipolar cycloadditions.
    Shi F, Tao ZL, Luo SW, Tu SJ, Gong LZ.
    Chemistry; 2012 May 29; 18(22):6885-94. PubMed ID: 22505189
    [Abstract] [Full Text] [Related]

  • 13. Asymmetric synthesis of spiro[isoxazolin-3,3'-oxindoles] via the catalytic 1,3-dipolar cycloaddition reaction of nitrile oxides.
    Lian X, Guo S, Wang G, Lin L, Liu X, Feng X.
    J Org Chem; 2014 Aug 15; 79(16):7703-10. PubMed ID: 25054839
    [Abstract] [Full Text] [Related]

  • 14. Asymmetric synthesis of 3,3'-spirooxindoles fused with cyclobutanes through organocatalytic formal [2 + 2] cycloadditions under H-bond-directing dienamine activation.
    Qi LW, Yang Y, Gui YY, Zhang Y, Chen F, Tian F, Peng L, Wang LX.
    Org Lett; 2014 Dec 19; 16(24):6436-9. PubMed ID: 25494171
    [Abstract] [Full Text] [Related]

  • 15. Stereocontrolled synthesis of spirooxindoles through Lewis acid-promoted [5 + 2]-annulation of chiral silyl alcohols.
    Zhang Y, Panek JS.
    Org Lett; 2009 Aug 06; 11(15):3366-9. PubMed ID: 19719185
    [Abstract] [Full Text] [Related]

  • 16. Diastereodivergent synthesis of 3-spirocyclopropyl-2-oxindoles through direct enantioselective cyclopropanation of oxindoles.
    Dou X, Lu Y.
    Chemistry; 2012 Jul 02; 18(27):8315-9. PubMed ID: 22674465
    [No Abstract] [Full Text] [Related]

  • 17. Catalytic Aldol-Cyclization Cascade of 3-Isothiocyanato Oxindoles with α-Ketophosphonates for the Enantioselective Synthesis of β-Amino-α-hydroxyphosphonates.
    Kayal S, Mukherjee S.
    Org Lett; 2015 Nov 06; 17(21):5508-11. PubMed ID: 26512732
    [Abstract] [Full Text] [Related]

  • 18. Highly diastereoselective one-pot synthesis of spirocyclic oxindoles through intramolecular Ullmann coupling and Claisen rearrangement.
    Miyamoto H, Okawa Y, Nakazaki A, Kobayashi S.
    Angew Chem Int Ed Engl; 2006 Mar 27; 45(14):2274-7. PubMed ID: 16518792
    [No Abstract] [Full Text] [Related]

  • 19. FeCl3-Mediated Radical Tandem Reactions of 3-Benzyl-2-oxindoles with Styrene Derivatives for the Stereoselective Synthesis of Spirocyclohexene Oxindoles.
    Wu HR, Cheng L, Kong DL, Huang HY, Gu CL, Liu L, Wang D, Li CJ.
    Org Lett; 2016 Mar 18; 18(6):1382-5. PubMed ID: 26950164
    [Abstract] [Full Text] [Related]

  • 20. Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: synthesis of 3-spirocyclopentene-2-oxindoles having two contiguous quaternary centers.
    Zhong F, Han X, Wang Y, Lu Y.
    Angew Chem Int Ed Engl; 2011 Aug 16; 50(34):7837-41. PubMed ID: 21728218
    [No Abstract] [Full Text] [Related]

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