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 *

181 related articles for article (PubMed ID: 21591768)

  • 41. 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]  

  • 42. Core structure-based design of organocatalytic [3+2]-cycloaddition reactions: highly efficient and stereocontrolled syntheses of 3,3'-pyrrolidonyl spirooxindoles.
    Tan B; Zeng X; Leong WW; Shi Z; Barbas CF; Zhong G
    Chemistry; 2012 Jan; 18(1):63-7. PubMed ID: 22162076
    [No Abstract]   [Full Text] [Related]  

  • 43. Domino Pd-catalyzed Heck cyclization and bismuth-catalyzed hydroamination: formal synthesis of elacomine and isoelacomine.
    Kamisaki H; Nanjo T; Tsukano C; Takemoto Y
    Chemistry; 2011 Jan; 17(2):626-33. PubMed ID: 21207582
    [TBL] [Abstract][Full Text] [Related]  

  • 44. N-Heterocyclic carbene-catalyzed [4 + 2] cyclization of α,β-unsaturated carboxylic acids bearing γ-H with isatins: an enantioselective synthesis of spirocyclic oxindole-dihydropyranones.
    Zhu L; Yu C; Li T; Wang Y; Lu Y; Wang W; Yao C
    Org Biomol Chem; 2016 Jan; 14(4):1485-91. PubMed ID: 26690686
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Catalytic enantioselective formal hetero-Diels-Alder reactions of enones with isatins to give spirooxindole tetrahydropyranones.
    Cui HL; Tanaka F
    Chemistry; 2013 May; 19(20):6213-6. PubMed ID: 23559482
    [TBL] [Abstract][Full Text] [Related]  

  • 46. TiCl4 catalyzed tandem construction of C-C and C-O bonds: a simple and one-pot atom-economical stereoselective synthesis of spiro-oxindoles.
    Basavaiah D; Rao JS; Reddy RJ; Rao AJ
    Chem Commun (Camb); 2005 May; (20):2621-3. PubMed ID: 15900347
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Total synthesis of (-)-reveromycin a.
    El Sous M; Ganame D; Tregloan PA; Rizzacasa MA
    Org Lett; 2004 Aug; 6(17):3001-4. PubMed ID: 15330668
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Unusual formal [4 + 2] cycloaddition of ethyl allenoate with arylidenoxindoles: synthesis of dihydropyran-fused indoles.
    Chen XY; Wen MW; Ye S; Wang ZX
    Org Lett; 2011 Mar; 13(5):1138-41. PubMed ID: 21302968
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis.
    Ramachary DB; Venkaiah C; Madhavachary R
    Org Lett; 2013 Jun; 15(12):3042-5. PubMed ID: 23724824
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Highly efficient and stereocontrolled construction of 3,3'-pyrrolidonyl spirooxindoles via organocatalytic domino Michael/cyclization reaction.
    Liu XL; Han WY; Zhang XM; Yuan WC
    Org Lett; 2013 Mar; 15(6):1246-9. PubMed ID: 23452297
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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; 19(5):1747-53. PubMed ID: 23255327
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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(6):1382-5. PubMed ID: 26950164
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Asymmetric quadruple aminocatalytic domino reactions to fused carbocycles incorporating a spirooxindole motif.
    Jiang K; Jia ZJ; Yin X; Wu L; Chen YC
    Org Lett; 2010 Jun; 12(12):2766-9. PubMed ID: 20481511
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds.
    Reddy BV; Gopal Reddy S; Ramana Reddy M; Pal Bhadra M; Sarma AV
    Org Biomol Chem; 2014 Oct; 12(37):7257-60. PubMed ID: 25103114
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Synthesis of highly functionalised spiro-indoles by a halogen atom transfer radical cyclization.
    Stevens CV; Van Meenen E; Eeckhout Y; Vanderhoydonck B; Hooghe W
    Chem Commun (Camb); 2005 Oct; (38):4827-9. PubMed ID: 16193128
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A tandem isomerization/prins strategy: iridium(III)/Brønsted acid cooperative catalysis.
    Lombardo VM; Thomas CD; Scheidt KA
    Angew Chem Int Ed Engl; 2013 Dec; 52(49):12910-4. PubMed ID: 24218144
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Magnetic, acidic, ionic liquid-catalyzed one-pot synthesis of spirooxindoles.
    Khalafi-Nezhad A; Mohammadi S
    ACS Comb Sci; 2013 Sep; 15(9):512-8. PubMed ID: 23971413
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. Chirality transfer in Au-catalyzed cyclization reactions of monoallylic diols: selective access to specific enantiomers based on olefin geometry.
    Aponick A; Biannic B
    Org Lett; 2011 Mar; 13(6):1330-3. PubMed ID: 21314106
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.