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Journal Abstract Search

180 related items for PubMed ID: 23112107

  • 1. Highly enantio- and diastereoselective generation of two quaternary centers in spirocyclopropanation of oxindole derivatives.
    Noole A, Sucman NS, Kabeshov MA, Kanger T, Macaev FZ, Malkov AV.
    Chemistry; 2012 Nov 19; 18(47):14929-33. PubMed ID: 23112107
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Diastereoselective synthesis of functionalized spirocyclopropyl oxindoles via P(NMe2)3-mediated reductive cyclopropanation.
    Zhou R, Yang C, Liu Y, Li R, He Z.
    J Org Chem; 2014 Nov 07; 79(21):10709-15. PubMed ID: 25333339
    [Abstract] [Full Text] [Related]

  • 4. Organocatalytic Michael-alkylation cascade: the enantioselective nitrocyclopropanation of oxindoles.
    Pesciaioli F, Righi P, Mazzanti A, Bartoli G, Bencivenni G.
    Chemistry; 2011 Mar 01; 17(10):2842-5. PubMed ID: 21308819
    [No Abstract] [Full Text] [Related]

  • 5. Highly efficient enantioselective construction of bispirooxindoles containing three stereocenters through an organocatalytic cascade Michael-cyclization reaction.
    Wu H, Zhang LL, Tian ZQ, Huang YD, Wang YM.
    Chemistry; 2013 Jan 28; 19(5):1747-53. PubMed ID: 23255327
    [Abstract] [Full Text] [Related]

  • 6. Enantio- and diastereoselective synthesis of spiro-epoxyoxindoles.
    Boucherif A, Yang QQ, Wang Q, Chen JR, Lu LQ, Xiao WJ.
    J Org Chem; 2014 May 02; 79(9):3924-9. PubMed ID: 24730463
    [Abstract] [Full Text] [Related]

  • 7. Diastereoselective Synthesis of Spirocyclopropanes under Mild Conditions via Formal [2 + 1] Cycloadditions Using 2,3-Dioxo-4-benzylidene-pyrrolidines.
    Li Y, Li QZ, Huang L, Liang H, Yang KC, Leng HJ, Liu Y, Shen XD, Gou XJ, Li JL.
    Molecules; 2017 Feb 22; 22(2):. PubMed ID: 28241452
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Brønsted acid catalyzed asymmetric diels-alder reactions: stereoselective construction of spiro[tetrahydrocarbazole-3,3'-oxindole] framework.
    Wang Y, Tu MS, Yin L, Sun M, Shi F.
    J Org Chem; 2015 Mar 20; 80(6):3223-32. PubMed ID: 25692214
    [Abstract] [Full Text] [Related]

  • 10. Enantioselective construction of spirooxindole derivatives through [3+2] annulation catalyzed by a bisthiourea as a multiple-hydrogen-bond donor.
    Shi Y, Lin A, Mao H, Mao Z, Li W, Hu H, Zhu C, Cheng Y.
    Chemistry; 2013 Feb 04; 19(6):1914-8. PubMed ID: 23281117
    [Abstract] [Full Text] [Related]

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  • 12. An asymmetric approach toward chiral multicyclic spirooxindoles from isothiocyanato oxindoles and unsaturated pyrazolones by a chiral tertiary amine thiourea catalyst.
    Chen Q, Liang J, Wang S, Wang D, Wang R.
    Chem Commun (Camb); 2013 Feb 25; 49(16):1657-9. PubMed ID: 23334197
    [Abstract] [Full Text] [Related]

  • 13. A new vinyl selenone-based domino approach to spirocyclopropyl oxindoles endowed with anti-HIV RT activity.
    Palomba M, Rossi L, Sancineto L, Tramontano E, Corona A, Bagnoli L, Santi C, Pannecouque C, Tabarrini O, Marini F.
    Org Biomol Chem; 2016 Feb 14; 14(6):2015-24. PubMed ID: 26754878
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
    Liu ZS, Li WK, Kang TR, He L, Liu QZ.
    Org Lett; 2015 Jan 02; 17(1):150-3. PubMed ID: 25525709
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Titanium(IV)-catalyzed stereoselective synthesis of spirooxindole-1-pyrrolines.
    Badillo JJ, Ribeiro CJ, Olmstead MM, Franz AK.
    Org Lett; 2014 Dec 19; 16(24):6270-3. PubMed ID: 25474118
    [Abstract] [Full Text] [Related]

  • 18. Asymmetric one-pot sequential Mannich/hydroamination reaction by organo- and gold catalysts: synthesis of spiro[pyrrolidin-3,2'-oxindole] derivatives.
    Chen X, Chen H, Ji X, Jiang H, Yao ZJ, Liu H.
    Org Lett; 2013 Apr 19; 15(8):1846-9. PubMed ID: 23560725
    [Abstract] [Full Text] [Related]

  • 19. Access to spirocyclic oxindoles via N-heterocyclic carbene-catalyzed reactions of enals and oxindole-derived α,β-unsaturated imines.
    Jiang K, Tiwari B, Chi YR.
    Org Lett; 2012 May 04; 14(9):2382-5. PubMed ID: 22524534
    [Abstract] [Full Text] [Related]

  • 20. Silver-promoted, palladium-catalyzed direct arylation of cyclopropanes: facile access to spiro 3,3'-cyclopropyl oxindoles.
    Ladd CL, Sustac Roman D, Charette AB.
    Org Lett; 2013 Mar 15; 15(6):1350-3. PubMed ID: 23452033
    [Abstract] [Full Text] [Related]

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