These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 22583112)

  • 21. N-heterocyclic carbene-catalyzed homoenolate additions with N-aryl ketimines as electrophiles: efficient synthesis of spirocyclic γ-lactam oxindoles.
    Zhang B; Feng P; Sun LH; Cui Y; Ye S; Jiao N
    Chemistry; 2012 Jul; 18(30):9198-203. PubMed ID: 22736551
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 17(20):5020-3. PubMed ID: 26412346
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The asymmetric synthesis of polycyclic 3-spirooxindole alkaloids via the cascade reaction of 2-isocyanoethylindoles.
    Zhao X; Liu X; Xiong Q; Mei H; Ma B; Lin L; Feng X
    Chem Commun (Camb); 2015 Nov; 51(89):16076-9. PubMed ID: 26389723
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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; 45(14):2274-7. PubMed ID: 16518792
    [No Abstract]   [Full Text] [Related]  

  • 25. Assembly of spirooxindole derivatives containing four consecutive stereocenters via organocatalytic Michael-Henry cascade reactions.
    Albertshofer K; Tan B; Barbas CF
    Org Lett; 2012 Apr; 14(7):1834-7. PubMed ID: 22436132
    [TBL] [Abstract][Full Text] [Related]  

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

  • 27. Alkaloid inspired spirocyclic oxindoles from 1,3-dipolar cycloaddition of pyridinium ylides.
    Day J; Uroos M; Castledine RA; Lewis W; McKeever-Abbas B; Dowden J
    Org Biomol Chem; 2013 Oct; 11(38):6502-9. PubMed ID: 23989496
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Multicomponent reaction to construct spirocyclic oxindoles with a Michael (triple Michael)/cyclization cascade sequence as the key step.
    Li J; Wang N; Li C; Jia X
    Chemistry; 2012 Jul; 18(31):9645-50. PubMed ID: 22815218
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 51(10):2448-51. PubMed ID: 22287059
    [No Abstract]   [Full Text] [Related]  

  • 30. 3-isothiocyanato oxindoles serving as powerful and versatile precursors to structurally diverse dispirocyclic thiopyrrolidineoxindoles through a cascade Michael/cyclization process with amino-thiocarbamate catalysts.
    Han WY; Li SW; Wu ZJ; Zhang XM; Yuan WC
    Chemistry; 2013 Apr; 19(18):5551-6. PubMed ID: 23495169
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 20(12):3415-20. PubMed ID: 24677230
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 16(24):6436-9. PubMed ID: 25494171
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 20(46):15047-52. PubMed ID: 25255976
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Synthesis of spirocarbamate oxindoles via intramolecular trapping of a β-silyl carbocation by an N-Boc group.
    Shupe BH; Allen EE; MacDonald JP; Wilson SO; Franz AK
    Org Lett; 2013 Jul; 15(13):3218-21. PubMed ID: 23758331
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Organocatalytic direct asymmetric aldol reactions of 3-isothiocyanato oxindoles to ketones: stereocontrolled synthesis of spirooxindoles bearing highly congested contiguous tetrasubstituted stereocenters.
    Chen WB; Wu ZJ; Hu J; Cun LF; Zhang XM; Yuan WC
    Org Lett; 2011 May; 13(9):2472-5. PubMed ID: 21473612
    [TBL] [Abstract][Full Text] [Related]  

  • 36. FeCl₃-catalyzed [3+3] annulation between 3-oxirane-indolin-2-ones and nitrones to construct spiro[1,4,2-dioxazinan]oxindoles.
    Yu J; Cai C
    Mol Divers; 2017 Aug; 21(3):761-768. PubMed ID: 28439765
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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; 18(22):6885-94. PubMed ID: 22505189
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 17(21):5508-11. PubMed ID: 26512732
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Assembly of spirooxindole derivatives containing four consecutive stereocenters by using cascade reactions catalyzed by an N-heterocyclic carbene.
    Zhou B; Luo Z; Li Y
    Chemistry; 2013 Apr; 19(14):4428-31. PubMed ID: 23467928
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Organocatalytic asymmetric desymmetrization: efficient construction of spirocyclic oxindoles bearing a unique all-carbon quaternary stereogenic center via sulfa-Michael addition.
    Yao L; Liu K; Tao HY; Qiu GF; Zhou X; Wang CJ
    Chem Commun (Camb); 2013 Jul; 49(54):6078-80. PubMed ID: 23728072
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.