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240 related items for PubMed ID: 11592876

  • 1. FR901464: total synthesis, proof of structure, and evaluation of synthetic analogues.
    Thompson CF, Jamison TF, Jacobsen EN.
    J Am Chem Soc; 2001 Oct 17; 123(41):9974-83. PubMed ID: 11592876
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  • 2. Enantioselective total syntheses of FR901464 and spliceostatin A and evaluation of splicing activity of key derivatives.
    Ghosh AK, Chen ZH, Effenberger KA, Jurica MS.
    J Org Chem; 2014 Jun 20; 79(12):5697-709. PubMed ID: 24873648
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  • 3. Stereoselective total synthesis of reveromycin B and C19-epi-reveromycin B.
    Drouet KE, Theodorakis EA.
    Chemistry; 2000 Jun 02; 6(11):1987-2001. PubMed ID: 10894398
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  • 4. Structure-activity relationship for FR901464: a versatile method for the conversion and preparation of biologically active biotinylated probes.
    Motoyoshi H, Horigome M, Ishigami K, Yoshida T, Horinouchi S, Yoshida M, Watanabe H, Kitahara T.
    Biosci Biotechnol Biochem; 2004 Oct 02; 68(10):2178-82. PubMed ID: 15502365
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  • 5. Total synthesis of the epidermal growth factor inhibitor (-)-reveromycin B.
    Cuzzupe AN, Hutton CA, Lilly MJ, Mann RK, McRae KJ, Zammit SC, Rizzacasa MA.
    J Org Chem; 2001 Apr 06; 66(7):2382-93. PubMed ID: 11281779
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  • 6. Convergent approach to complex spirocyclic pyrans: practical synthesis of the oxa-pinnaic acid core.
    Ferrari FD, Pasqua AE, Ledgard AJ, Marquez R.
    Org Biomol Chem; 2013 Jun 07; 11(21):3469-76. PubMed ID: 23589153
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  • 12. Antitumor compounds based on a natural product consensus pharmacophore.
    Lagisetti C, Pourpak A, Jiang Q, Cui X, Goronga T, Morris SW, Webb TR.
    J Med Chem; 2008 Oct 09; 51(19):6220-4. PubMed ID: 18788726
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  • 13. New antitumor substances, FR901463, FR901464 and FR901465. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities.
    Nakajima H, Sato B, Fujita T, Takase S, Terano H, Okuhara M.
    J Antibiot (Tokyo); 1996 Dec 09; 49(12):1196-203. PubMed ID: 9031664
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  • 17. Total syntheses, fragmentation studies, and antitumor/antiproliferative activities of FR901464 and its low picomolar analogue.
    Albert BJ, Sivaramakrishnan A, Naka T, Czaicki NL, Koide K.
    J Am Chem Soc; 2007 Mar 07; 129(9):2648-59. PubMed ID: 17279752
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  • 19. Total synthesis of the proposed structure for spirofungin B: a reassignment of the stereochemistry.
    Zanatta SD, White JM, Rizzacasa MA.
    Org Lett; 2004 Mar 18; 6(6):1041-4. PubMed ID: 15012095
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  • 20. Synthesis and stereochemistry of the terminal spiroketal domain of the phosphatase inhibitor dinophysistoxin-2.
    Forsyth CJ, Wang C.
    Bioorg Med Chem Lett; 2008 May 15; 18(10):3043-6. PubMed ID: 18226903
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