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Journal Abstract Search

254 related items for PubMed ID: 25333339

  • 1. 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
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  • 2. 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
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  • 3. 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
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  • 8. Pd(II)-Catalyzed Asymmetric Addition of Arylboronic Acids to Isatin-Derived Ketimines.
    He Q, Wu L, Kou X, Butt N, Yang G, Zhang W.
    Org Lett; 2016 Jan 15; 18(2):288-91. PubMed ID: 26720106
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  • 9. Asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene.
    Dou X, Yao W, Zhou B, Lu Y.
    Chem Commun (Camb); 2013 Oct 14; 49(80):9224-6. PubMed ID: 23995624
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  • 11. Unprecedented one-pot, domino tertiary alcohol protection-Michael type addition of halides to Morita-Baylis-Hillman adduct of isatin with RCOX/K2CO3: diastereoselective synthesis of oxindole appended β-halo esters.
    Solaiselvi R, Shanmugam P, Mandal AB.
    Org Lett; 2013 Mar 15; 15(6):1186-9. PubMed ID: 23461280
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  • 12. trans-Directing ability of amide groups in cyclopropanation: application to the asymmetric cyclopropanation of alkenes with diazo reagents bearing two carboxy groups.
    Marcoux D, Charette AB.
    Angew Chem Int Ed Engl; 2008 Mar 15; 47(52):10155-8. PubMed ID: 19035611
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  • 14. Synthesis of Chiral Spiro-Aziridine Oxindoles via Aza-Corey-Chaykovsky Reaction of Isatin Derived N-tert-Butanesulfinyl Ketimines.
    Hajra S, Aziz SM, Jana B, Mahish P, Das D.
    Org Lett; 2016 Feb 05; 18(3):532-5. PubMed ID: 26781920
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  • 19. 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
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  • 20. A highly diastereoselective Friedel-Crafts reaction of indoles with isatin-derived N-sulfinyl ketimines towards the efficient synthesis of chiral tetrasubstituted 3-indolyl-3-aminooxindoles.
    Chen JP, Chen WW, Li Y, Xu MH.
    Org Biomol Chem; 2015 Mar 21; 13(11):3363-70. PubMed ID: 25655031
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