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263 related items for PubMed ID: 26473557

  • 1. Synthesis of Lamellarin D Trimethyl Ether and Lamellarin H via 6π-Electrocyclization.
    Dialer C, Imbri D, Hansen SP, Opatz T.
    J Org Chem; 2015 Nov 20; 80(22):11605-10. PubMed ID: 26473557
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  • 4. Scalable Total Syntheses of Some Natural and Unnatural Lamellarins: Application of a One-Pot Domino Process for Regioselective Access to the Central 1,2,4-Trisubstituted Pyrrole Core.
    Kumar V, Awasthi A, Salam A, Khan T.
    J Org Chem; 2019 Sep 20; 84(18):11596-11603. PubMed ID: 31433662
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  • 6. Synthesis of lamellarin U and lamellarin G trimethyl ether by alkylation of a deprotonated alpha-aminonitrile.
    Liermann JC, Opatz T.
    J Org Chem; 2008 Jun 20; 73(12):4526-31. PubMed ID: 18500839
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  • 8. Total synthesis of lamellarins D, H, and R and ningalin B.
    Li Q, Jiang J, Fan A, Cui Y, Jia Y.
    Org Lett; 2011 Jan 21; 13(2):312-5. PubMed ID: 21175172
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  • 9. Design and synthesis of lamellarin D analogues targeting topoisomerase I.
    Ohta T, Fukuda T, Ishibashi F, Iwao M.
    J Org Chem; 2009 Nov 06; 74(21):8143-53. PubMed ID: 19791738
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  • 10. Total synthesis of natural and unnatural lamellarins with saturated and unsaturated D-rings.
    Ploypradith P, Petchmanee T, Sahakitpichan P, Litvinas ND, Ruchirawat S.
    J Org Chem; 2006 Dec 08; 71(25):9440-8. PubMed ID: 17137371
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  • 13. A modular synthesis of the lamellarins: total synthesis of lamellarin G trimethyl ether.
    Handy ST, Zhang Y, Bregman H.
    J Org Chem; 2004 Apr 02; 69(7):2362-6. PubMed ID: 15049631
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  • 14. Pyrrolo[2,1-alpha]isoquinoline as a skeleton for the synthesis of bioactive lamellarin H.
    You YC, Wang AL, Li DP, Yang G.
    Biomed Mater; 2006 Sep 02; 1(3):L7-9. PubMed ID: 18458386
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  • 15. Synthesis and structure-activity relationship study of potent cytotoxic analogues of the marine alkaloid Lamellarin D.
    Pla D, Marchal A, Olsen CA, Francesch A, Cuevas C, Albericio F, Alvarez M.
    J Med Chem; 2006 Jun 01; 49(11):3257-68. PubMed ID: 16722644
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  • 16. Topoisomerase I-mediated DNA cleavage as a guide to the development of antitumor agents derived from the marine alkaloid lamellarin D: triester derivatives incorporating amino acid residues.
    Tardy C, Facompré M, Laine W, Baldeyrou B, García-Gravalos D, Francesch A, Mateo C, Pastor A, Jiménez JA, Manzanares I, Cuevas C, Bailly C.
    Bioorg Med Chem; 2004 Apr 01; 12(7):1697-712. PubMed ID: 15028262
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  • 19. Synthesis of chromeno[3,4-b]indoles as Lamellarin D analogues: a novel DYRK1A inhibitor class.
    Neagoie C, Vedrenne E, Buron F, Mérour JY, Rosca S, Bourg S, Lozach O, Meijer L, Baldeyrou B, Lansiaux A, Routier S.
    Eur J Med Chem; 2012 Mar 01; 49():379-96. PubMed ID: 22305342
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