BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

637 related articles for article (PubMed ID: 29510590)

  • 1. 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]  

  • 2. Synthesis of pyrrolo(spiro-[2.3']-oxindole)-spiro-[4.3"]-oxindole via 1,3-dipolar cycloaddition of azomethine ylides with 3-acetonylideneoxindole.
    Xiao JA; Zhang HG; Liang S; Ren JW; Yang H; Chen XQ
    J Org Chem; 2013 Nov; 78(22):11577-83. PubMed ID: 24111532
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of novel functionalized 3-spiropyrrolizidine and 3-spiropyrrolidine oxindoles from Baylis-Hillman adducts of isatin and heteroaldehydes with azomethine ylides via [3+2]-cycloaddition.
    Shanmugam P; Viswambharan B; Madhavan S
    Org Lett; 2007 Oct; 9(21):4095-8. PubMed ID: 17877359
    [TBL] [Abstract][Full Text] [Related]  

  • 4. exo-Selective construction of spiro-[butyrolactone-pyrrolidine] via 1,3-dipolar cycloaddition of azomethine ylides with α-methylene-γ-butyrolactone catalyzed by Cu(I)/DTBM-BIPHEP.
    Li QH; Liu TL; Wei L; Zhou X; Tao HY; Wang CJ
    Chem Commun (Camb); 2013 Oct; 49(83):9642-4. PubMed ID: 24022250
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Catalytic asymmetric construction of spiro[pyrrolidine-2,3'-oxindole] scaffolds through chiral phosphoric acid-catalyzed 1,3-dipolar cycloaddition involving 3-amino oxindoles.
    Zhu G; Wang B; Bao X; Zhang H; Wei Q; Qu J
    Chem Commun (Camb); 2015 Nov; 51(85):15510-3. PubMed ID: 26345264
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The copper-catalyzed asymmetric construction of a dispiropyrrolidine skeleton via 1,3-dipolar cycloaddition of azomethine ylides to α-alkylidene succinimides.
    Yang WL; Liu YZ; Luo S; Yu X; Fossey JS; Deng WP
    Chem Commun (Camb); 2015 Jun; 51(44):9212-5. PubMed ID: 25952504
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. [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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Regioselective synthesis of novel spiropyrrolidines and spirothiapyrrolizidines through multicomponent 1,3-dipolar cycloaddition reaction of azomethine ylides.
    Liu H; Dou G; Shi D
    J Comb Chem; 2010 Sep; 12(5):633-7. PubMed ID: 20608736
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Organocatalytic synthesis of spiro[pyrrolidin-3,3'-oxindoles] with high enantiopurity and structural diversity.
    Chen XH; Wei Q; Luo SW; Xiao H; Gong LZ
    J Am Chem Soc; 2009 Sep; 131(38):13819-25. PubMed ID: 19736987
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multicomponent Dipolar Cycloaddition Strategy: Combinatorial Synthesis of Novel Spiro-Tethered Pyrazolo[3,4-b]quinoline Hybrid Heterocycles.
    Sumesh RV; Muthu M; Almansour AI; Suresh Kumar R; Arumugam N; Athimoolam S; Jeya Yasmi Prabha EA; Kumar RR
    ACS Comb Sci; 2016 May; 18(5):262-70. PubMed ID: 27027478
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Asymmetric synthesis of spiro[isoxazolin-3,3'-oxindoles] via the catalytic 1,3-dipolar cycloaddition reaction of nitrile oxides.
    Lian X; Guo S; Wang G; Lin L; Liu X; Feng X
    J Org Chem; 2014 Aug; 79(16):7703-10. PubMed ID: 25054839
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction.
    Haddad S; Boudriga S; Porzio F; Soldera A; Askri M; Knorr M; Rousselin Y; Kubicki MM; Golz C; Strohmann C
    J Org Chem; 2015 Sep; 80(18):9064-75. PubMed ID: 26291879
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spiro[pyrrolidine-2,3'-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions.
    Chen G; Yang J; Gao S; He H; Li S; Di Y; Chang Y; Lu Y; Hao X
    Mol Divers; 2012 Feb; 16(1):151-6. PubMed ID: 22134725
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ultrasound-promoted synthesis of novel spirooxindolo/spiroacenaphthen dicyano pyrrolidines and pyrrolizidines through regioselective azomethine ylide cycloaddition reaction.
    Tabatabaei Rezaei SJ; Nabid MR; Yari A; Ng SW
    Ultrason Sonochem; 2011 Jan; 18(1):49-53. PubMed ID: 20692198
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The discovery of oxazolones-grafted spirooxindoles via three-component diversity oriented synthesis and their preliminary biological evaluation.
    Dong H; Song S; Li J; Xu C; Zhang H; Ouyang L
    Bioorg Med Chem Lett; 2015 Sep; 25(17):3585-91. PubMed ID: 26159483
    [TBL] [Abstract][Full Text] [Related]  

  • 20. One-Pot Access to a Library of Dispiro Oxindole-pyrrolidine/pyrrolothiazole-thiochromane Hybrids via Three-Component 1,3-Dipolar Cycloaddition Reactions.
    Uma Rani G; Vivek Kumar S; Bharkavi C; Menéndez JC; Perumal S
    ACS Comb Sci; 2016 Jun; 18(6):337-42. PubMed ID: 27073991
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.