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 *

89 related articles for article (PubMed ID: 24746140)

  • 1. Convenient synthesis of triphenylphosphanylidene spiro[cyclopentane-1,3'-indolines] and spiro[cyclopent[3]ene-1,3'-indolines] via three-component reactions. [Corrected].
    Han Y; Sheng YJ; Yan CG
    Org Lett; 2014 May; 16(10):2654-7. PubMed ID: 24746140
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Correction to "Convenient Synthesis of Triphenylphosphanylidene Spiro[cyclopentane-1,3'-indolines] and Spiro[cyclopent[2]ene-1,3'-indolines] via Three-Component Reactions".
    Han Y; Sheng YJ; Yan CG
    Org Lett; 2015 Nov; 17(21):5516. PubMed ID: 26484584
    [No Abstract]   [Full Text] [Related]  

  • 3. Tri(
    Zheng H; Han Y; Sun J; Yan CG
    Beilstein J Org Chem; 2022; 18():669-679. PubMed ID: 35821699
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diastereoselective synthesis of spiro[benzo[d]pyrrolo[2,1-b]thiazole-3,3'-indolines] via cycloaddition reaction of N-phenacylbenzothiazolium bromides and 3-methyleneoxindoles.
    Shen GL; Sun J; Yan CG
    Org Biomol Chem; 2015 Nov; 13(44):10929-38. PubMed ID: 26373777
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis of functionalized spiro[indoline-3,4'-pyridines] and spiro[indoline-3,4'-pyridinones] via one-pot four-component reactions.
    Zhang LJ; Wu Q; Sun J; Yan CG
    Beilstein J Org Chem; 2013; 9():846-51. PubMed ID: 23766799
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diastereoselective construction of carbazole-based spirooxindoles via the Levy three-component reaction.
    Zhan SC; Sun J; Liu RZ; Yan CG
    Org Biomol Chem; 2019 Dec; 18(1):163-168. PubMed ID: 31808499
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis of spiro[dihydropyridine-oxindoles] via three-component reaction of arylamine, isatin and cyclopentane-1,3-dione.
    Sun Y; Sun J; Yan CG
    Beilstein J Org Chem; 2013; 9():8-14. PubMed ID: 23399791
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Convenient synthesis of functionalized spiro[indoline-3,2'-pyrrolizines] or spiro[indoline-3,3'-pyrrolidines] via multicomponent reactions.
    Sun J; Chen L; Gong H; Yan CG
    Org Biomol Chem; 2015 Jun; 13(21):5905-17. PubMed ID: 25921751
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Formation of diverse polycyclic spirooxindoles via three-component reaction of isoquinolinium salts, isatins and malononitrile.
    Sun J; Shen GL; Huang Y; Yan CG
    Sci Rep; 2017 Jan; 7():41024. PubMed ID: 28106130
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Selective Construction of Diverse Polycyclic Spirooxindoles via a Three-Component Reaction of Cyclic Mercapto-Substituted β-Enamino Esters, Isatins, and Cyclic 1,3-Diketones.
    Sun QS; Sun J; Pan LN; Yan CG
    J Org Chem; 2020 Oct; 85(19):12117-12127. PubMed ID: 32901479
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis of functionalized dispiro[indoline-3,1[Formula: see text]-cyclopentane-3[Formula: see text],3[Formula: see text]-indolines] via cyclodimerization of 3-phenacylideneoxindolines with benzoylhydrazides and arylhydrazines.
    Yang RY; Sun J; Jin G; Yan CG
    Mol Divers; 2018 Feb; 22(1):21-36. PubMed ID: 29058229
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copper-catalyzed multicomponent reactions for the efficient synthesis of diverse spirotetrahydrocarbazoles.
    Zhan SC; Fang RJ; Sun J; Yan CG
    Beilstein J Org Chem; 2022; 18():796-808. PubMed ID: 35875709
    [TBL] [Abstract][Full Text] [Related]  

  • 13. One-pot four-component reaction for convenient synthesis of functionalized 1-benzamidospiro[indoline-3,4'-pyridines].
    Wang C; Jiang YH; Yan CG
    Beilstein J Org Chem; 2014; 10():2671-6. PubMed ID: 25550730
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Selective synthesis of tetrahydroimidazo[1,2-a]pyridine and pyrrolidine derivatives via a one-pot two-step reaction.
    Zhang Y; Sun J; Shen GL; Yan CG
    Org Biomol Chem; 2017 Oct; 15(38):8072-8077. PubMed ID: 28905062
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Asymmetric Synthesis of Spiro[Azetidine-3,3'-Indoline]-2,2'-Diones via Copper(I)-Catalyzed Kinugasa/C-C Coupling Cascade Reaction.
    Zhong X; Huang M; Xiong H; Liang Y; Zhou W; Cai Q
    Angew Chem Int Ed Engl; 2022 Oct; 61(42):e202208323. PubMed ID: 36053546
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A consecutive synthesis of spiro[cyclopenta[b]pyrrole-5,2'-indene] derivatives via spirocyclization/annulation reactions.
    Parhami A; Yavari I; Najafi GR
    Mol Divers; 2023 Oct; 27(5):2001-2013. PubMed ID: 36224502
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Selective synthesis of functionalized spiro[indoline-3,2'-pyridines] and spiro[indoline-3,4'-pyridines] by Lewis acid catalyzed reactions of acetylenedicarboxylate, arylamines, and isatins.
    Gao H; Sun J; Yan CG
    J Org Chem; 2014 May; 79(9):4131-6. PubMed ID: 24693861
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Construction of Diverse Fused Chromene Frameworks via Isocyanide-Based Three-Component Reaction.
    He YW; Huang L; Huang K; Yan CG; Sun J; Han Y
    J Org Chem; 2024 Jul; ():. PubMed ID: 38993063
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Base controlled rongalite-mediated reductive aldol/cyclization and dimerization of isatylidene malononitriles/cyanoacetates.
    Chaudhari SS; Nichinde CB; Patil BR; Girase AS; Rama Krishna G; Kinage AK
    Org Biomol Chem; 2024 Feb; 22(8):1727-1732. PubMed ID: 38318869
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Organocatalyzed [4 + 2] cycloaddition of α,β-unsaturated ketones and isatylidene malononitrile: accessing spiro[3-arylcyclohexanone]oxindole derivatives.
    Patil BR; Nichinde CB; Chaudhari SS; Krishna GR; Kinage AK
    RSC Adv; 2024 Jan; 14(5):2873-2877. PubMed ID: 38239455
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.