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 *

163 related articles for article (PubMed ID: 36157552)

  • 1. Three-Component [3+2] Cycloaddition for Regio- and Diastereoselective Synthesis of Spirooxindole-Pyrrolidines.
    Zhang X; Liu M; Zhan D; Kaur M; Jasinski JP; Zhang W
    New J Chem; 2022 Feb; 46(8):3866-3870. PubMed ID: 36157552
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Facile One-Pot Construction of Succinimide-Fused Spiro[Pyrrolidine-2,3'-Oxindoles] via 1,3-Dipolar Cycloaddition Involving 3-Amino Oxindoles and Maleimides.
    Jin L; Liang F
    Molecules; 2018 Mar; 23(3):. PubMed ID: 29510590
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 1,3-Dipolar Cycloaddition of Isatin-Derived Azomethine Ylides with 2 H-Azirines: Stereoselective Synthesis of 1,3-Diazaspiro[bicyclo[3.1.0]hexane]oxindoles.
    Angyal A; Demjén A; Harmat V; Wölfling J; Puskás LG; Kanizsai I
    J Org Chem; 2019 Apr; 84(7):4273-4281. PubMed ID: 30860375
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis.
    Narayan R; Potowski M; Jia ZJ; Antonchick AP; Waldmann H
    Acc Chem Res; 2014 Apr; 47(4):1296-310. PubMed ID: 24730692
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments.
    Miankooshki FR; Bayat M; Nasri S; Samet NH
    Mol Divers; 2023 Oct; 27(5):2365-2397. PubMed ID: 35925529
    [TBL] [Abstract][Full Text] [Related]  

  • 6. One-pot double annulations to confer diastereoselective spirooxindolepyrrolothiazoles.
    Lu J; Yao B; Zhan D; Sun Z; Ji Y; Zhang X
    Beilstein J Org Chem; 2022; 18():1607-1616. PubMed ID: 36530533
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pseudo-Five-Component Reaction for Diastereoselective Synthesis of Butterfly Shaped Bispiro[Oxindole-Pyrrolidine]s.
    Zhang X; Qiu W; Murray SA; Zhan D; Evans J; Jasinski JP; Wang X; Zhang W
    J Org Chem; 2021 Dec; 86(23):17395-17403. PubMed ID: 34797667
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Bmim]Br Accelerated One-Pot Three-Component Cascade Protocol for the Construction of Spirooxindole-Pyrrolidine Heterocyclic Hybrids.
    Kumar RS; M Al-Thamili D; Almansour AI; Arumugam N; Dege N
    Molecules; 2020 Oct; 25(20):. PubMed ID: 33080968
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Double 1,3-Dipolar Cycloadditions of Two Nonstabilized Azomethine Ylides for Polycyclic Pyrrolidines.
    Zhang X; Qiu W; Evans J; Kaur M; Jasinski JP; Zhang W
    Org Lett; 2019 Apr; 21(7):2176-2179. PubMed ID: 30883128
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Combinatorial synthesis of functionalized spirooxindole-pyrrolidine/pyrrolizidine/pyrrolothiazole derivatives via three-component 1,3-dipolar cycloaddition reactions.
    Li J; Wang J; Xu Z; Zhu S
    ACS Comb Sci; 2014 Sep; 16(9):506-12. PubMed ID: 25033950
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Diastereoselective Synthesis of Dispiro[oxindole-cyclohexanone]pyrrolidines by 1,3-Dipolar Cycloaddition.
    Anis'kov A; Klochkova I; Tumskiy R; Yegorova A
    Molecules; 2017 Dec; 22(12):. PubMed ID: 29207519
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis, antidiabetic activity and molecular docking study of rhodanine-substitued spirooxindole pyrrolidine derivatives as novel α-amylase inhibitors.
    Toumi A; Boudriga S; Hamden K; Sobeh M; Cheurfa M; Askri M; Knorr M; Strohmann C; Brieger L
    Bioorg Chem; 2021 Jan; 106():104507. PubMed ID: 33288322
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Straightforward Regio- and Diastereoselective Synthesis, Molecular Structure, Intermolecular Interactions and Mechanistic Study of Spirooxindole-Engrafted Rhodanine Analogs.
    Barakat A; Haukka M; Soliman SM; Ali M; Al-Majid AM; El-Faham A; Domingo LR
    Molecules; 2021 Nov; 26(23):. PubMed ID: 34885853
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis of benzosuberone-tethered spirooxindoles: 1-3-dipolar cycloaddition of azomethine ylides and arylidene benzosuberones.
    Kumar SV; Rani GU; Divyalakshmi M; Bhuvanesh N; Muthusubramanian S; Perumal S
    Mol Divers; 2019 Aug; 23(3):669-680. PubMed ID: 30535898
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Catalytic asymmetric 1,3-dipolar cycloaddition of N-unprotected 2-oxoindolin-3-ylidene derivatives and azomethine ylides for the construction of spirooxindole-pyrrolidines.
    Liu TL; Xue ZY; Tao HY; Wang CJ
    Org Biomol Chem; 2011 Mar; 9(6):1980-6. PubMed ID: 21270976
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of highly functionalized pyrrolidines via a mild one-pot, three-component 1,3-dipolar cycloaddition process.
    Garner P; Kaniskan HU
    J Org Chem; 2005 Dec; 70(26):10868-71. PubMed ID: 16356011
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis of Functionalized 3-Spiro[cyclopropa[a]pyrrolizine]- and 3-Spiro[3-azabicyclo[3.1.0]hexane]oxindoles from Cyclopropenes and Azomethine Ylides via [3 + 2]-Cycloaddition.
    Filatov AS; Knyazev NA; Molchanov AP; Panikorovsky TL; Kostikov RR; Larina AG; Boitsov VM; Stepakov AV
    J Org Chem; 2017 Jan; 82(2):959-975. PubMed ID: 28004934
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Asymmetric [3 + 2] Cycloaddition of 3-Amino Oxindole-Based Azomethine Ylides and α,β-Enones with Divergent Diastereocontrol on the Spiro[pyrrolidine-oxindoles].
    Zhu G; Wei Q; Chen H; Zhang Y; Shen W; Qu J; Wang B
    Org Lett; 2017 Apr; 19(7):1862-1865. PubMed ID: 28349684
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Copper(I) catalyzed diastereoselective multicomponent synthesis of spiroindolo-pyrrolidines/-imidazolidines/-triazolidines from diazoamides via azomethine ylides.
    Muthusamy S; Kumar SG
    Org Biomol Chem; 2016 Feb; 14(7):2228-40. PubMed ID: 26786749
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Concise Total Synthesis of (-)-Quinocarcin Enabled by Catalytic Enantioselective Reductive 1,3-Dipolar Cycloaddition of Secondary Amides.
    Ji KL; He SF; Xu DD; He WX; Zheng JF; Huang PQ
    Angew Chem Int Ed Engl; 2023 Jun; 62(25):e202302832. PubMed ID: 37025034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.