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Journal Abstract Search

166 related items for PubMed ID: 21247215

  • 1.
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  • 2. Synthesis of the C1-C17 segment of phorboxazole B.
    Lucas BS, Luther LM, Burke SD.
    Org Lett; 2004 Aug 19; 6(17):2965-8. PubMed ID: 15330659
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  • 3. Total synthesis of the marine toxin phorboxazole A using palladium(II)-mediated intramolecular alkoxycarbonylation for tetrahydropyran synthesis.
    Kuntiyong P, Lee TH, Kranemann CL, White JD.
    Org Biomol Chem; 2012 Oct 21; 10(39):7884-99. PubMed ID: 22910851
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  • 5. (+)-Phorboxazole A synthetic studies. A highly convergent, second generation total synthesis of (+)-phorboxazole A.
    Smith AB, Razler TM, Ciavarri JP, Hirose T, Ishikawa T.
    Org Lett; 2005 Sep 29; 7(20):4399-402. PubMed ID: 16178543
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  • 6. Intramolecular palladium(II)-mediated alkoxy carbonylation as a route to functionalized tetrahydropyrans. Synthesis of the C9-C32 segment of phorboxazole A.
    White JD, Kranemann CL, Kuntiyong P.
    Org Lett; 2001 Dec 13; 3(25):4003-6. PubMed ID: 11735570
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  • 13. Total synthesis of phorboxazole A.
    Williams DR, Kiryanov AA, Emde U, Clark MP, Berliner MA, Reeves JT.
    Angew Chem Int Ed Engl; 2003 Mar 17; 42(11):1258-62. PubMed ID: 12645057
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  • 14. An approach to the bis-oxazole macrocycle of diazonamides.
    Zhang J, Ciufolini MA.
    Org Lett; 2011 Feb 04; 13(3):390-3. PubMed ID: 21174393
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  • 18. Total synthesis of (+)-phorboxazole A, a potent cytostatic agent from the sponge Phorbas sp.
    Pattenden G, González MA, Little PB, Millan DS, Plowright AT, Tornos JA, Ye T.
    Org Biomol Chem; 2003 Dec 07; 1(23):4173-208. PubMed ID: 14685321
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  • 19. Phorboxazole synthetic studies. 2. Construction of a C(20-28) subtarget, a further extension of the Petasis-Ferrier rearrangement.
    Smith AB, Minbiole KP, Verhoest PR, Beauchamp TJ.
    Org Lett; 1999 Sep 23; 1(6):913-6. PubMed ID: 10823222
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  • 20. Design and synthesis of a potent phorboxazole C(11-15) acetal analogue.
    Smith AB, Razler TM, Meis RM, Pettit GR.
    Org Lett; 2006 Feb 16; 8(4):797-9. PubMed ID: 16468770
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