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147 related items for PubMed ID: 11263923

  • 1. An aldol approach to the synthesis of the EF fragment of spongistatin 1.
    Crimmins MT, Katz JD, McAtee LC, Tabet EA, Kirincich SJ.
    Org Lett; 2001 Mar 22; 3(6):949-52. PubMed ID: 11263923
    [Abstract] [Full Text] [Related]

  • 2. Synthesis of the C29-C44 portion of spongistatin 1 (altohyrtin A).
    Wallace GA, Scott RW, Heathcock CH.
    J Org Chem; 2000 Jun 30; 65(13):4145-52. PubMed ID: 10866633
    [Abstract] [Full Text] [Related]

  • 3. Asymmetric total synthesis of spongistatins 1 and 2.
    Crimmins MT, Katz JD, Washburn DG, Allwein SP, McAtee LF.
    J Am Chem Soc; 2002 May 22; 124(20):5661-3. PubMed ID: 12010038
    [Abstract] [Full Text] [Related]

  • 4. Synthesis of the C16-C28 spiroketal subunit of spongistatin 1 (altohyrtin A): the pyrone approach.
    Crimmins MT, Katz JD.
    Org Lett; 2000 Apr 06; 2(7):957-60. PubMed ID: 10768196
    [Abstract] [Full Text] [Related]

  • 5. Total synthesis of (+)-spongistatin 1. An effective second-generation construction of an advanced EF Wittig salt, fragment union, and final elaboration.
    Smith AB, Zhu W, Shirakami S, Sfouggatakis C, Doughty VA, Bennett CS, Sakamoto Y.
    Org Lett; 2003 Mar 06; 5(5):761-4. PubMed ID: 12605509
    [Abstract] [Full Text] [Related]

  • 6. Spongistatin synthetic studies. An efficient, second-generation construction of an advanced ABCD intermediate.
    Smith AB, Doughty VA, Sfouggatakis C, Bennett CS, Koyanagi J, Takeuchi M.
    Org Lett; 2002 Mar 07; 4(5):783-6. PubMed ID: 11869127
    [Abstract] [Full Text] [Related]

  • 7. Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals.
    Holson EB, Roush WR.
    Org Lett; 2002 Oct 17; 4(21):3723-5. PubMed ID: 12375928
    [Abstract] [Full Text] [Related]

  • 8. Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reaction.
    Holson EB, Roush WR.
    Org Lett; 2002 Oct 17; 4(21):3719-22. PubMed ID: 12375927
    [Abstract] [Full Text] [Related]

  • 9. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the southern hemisphere EF segment.
    Paterson I, Coster MJ, Chen DY, Aceña JL, Bach J, Keown LE, Trieselmann T.
    Org Biomol Chem; 2005 Jul 07; 3(13):2420-30. PubMed ID: 15976859
    [Abstract] [Full Text] [Related]

  • 10. Anti aldol selectivity in a synthetic approach to the C1-C12 fragment of the tedanolides.
    Jung ME, Zhang TH.
    Org Lett; 2008 Jan 03; 10(1):137-40. PubMed ID: 18067310
    [Abstract] [Full Text] [Related]

  • 11. Halichondrin B: synthesis of the C(1)-C(15) subunit.
    Burke SD, Jung KW, Lambert WT, Phillips JR, Klovning JJ.
    J Org Chem; 2000 Jun 30; 65(13):4070-87. PubMed ID: 10866625
    [Abstract] [Full Text] [Related]

  • 12. Synthesis of the C1-C12 fragment of the tedanolides. Aldol-non-aldol aldol approach.
    Jung ME, Yoo D.
    Org Lett; 2007 Aug 30; 9(18):3543-6. PubMed ID: 17676748
    [Abstract] [Full Text] [Related]

  • 13. A modular approach to marine macrolide construction. 3. Enantioselective synthesis of the C1-C28 sector of spongistatin 1 (altohyrtin A).
    Zuev D, Paquette LA.
    Org Lett; 2000 Mar 09; 2(5):679-82. PubMed ID: 10814408
    [Abstract] [Full Text] [Related]

  • 14. Spongistatin synthetic studies. evolution of a scalable synthesis for the EF fragment of (+)-Spongistatin 1 exploiting a Petasis-Ferrier union/rearrangement tactic.
    Smith AB, Sfouggatakis C, Gotchev DB, Shirakami S, Bauer D, Zhu W, Doughty VA.
    Org Lett; 2004 Sep 30; 6(20):3637-40. PubMed ID: 15387567
    [Abstract] [Full Text] [Related]

  • 15. Asymmetric synthesis of the northern half C1-C16 of the bryostatins.
    Vakalopoulos A, Lampe TF, Hoffmann HM.
    Org Lett; 2001 Mar 22; 3(6):929-32. PubMed ID: 11263918
    [Abstract] [Full Text] [Related]

  • 16. Synthesis of the C(29)-C(45) bis-pyran subunit (E-F) of spongistatin 1 (Altohyrtin A).
    Micalizio GC, Pinchuk AN, Roush WR.
    J Org Chem; 2000 Dec 15; 65(25):8730-6. PubMed ID: 11112596
    [Abstract] [Full Text] [Related]

  • 17. Synthesis of a C(29)-C(51) subunit of spongistatin 1 (Altohyrtin A) starting from (R)-3-benzyloxy-2-methylpropan-1-ol.
    Lemaire-Audoire S, Vogel P.
    J Org Chem; 2000 Jun 02; 65(11):3346-56. PubMed ID: 10843616
    [Abstract] [Full Text] [Related]

  • 18. Studies directed toward the total synthesis of discodermolide: asymmetric synthesis of the C1-C14 fragment.
    Arefolov A, Panek JS.
    Org Lett; 2002 Jul 11; 4(14):2397-400. PubMed ID: 12098256
    [Abstract] [Full Text] [Related]

  • 19. Multigram synthesis of the C29-C51 subunit and completion of the total synthesis of altohyrtin C (spongistatin 2).
    Heathcock CH, McLaughlin M, Medina J, Hubbs JL, Wallace GA, Scott R, Claffey MM, Hayes CJ, Ott GR.
    J Am Chem Soc; 2003 Oct 22; 125(42):12844-9. PubMed ID: 14558833
    [Abstract] [Full Text] [Related]

  • 20. Structure-based design of a novel synthetic spiroketal pyran as a pharmacophore for the marine natural product spongistatin 1.
    Uckun FM, Mao C, Vassilev AO, Huang H, Jan ST.
    Bioorg Med Chem Lett; 2000 Mar 20; 10(6):541-5. PubMed ID: 10741549
    [Abstract] [Full Text] [Related]

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