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PUBMED FOR HANDHELDS

Journal Abstract Search


428 related items for PubMed ID: 15932193

  • 1.
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  • 2. Stereoselective synthesis of premisakinolide A, the monomeric counterpart of the marine 40-membered dimeric macrolide misakinolide A.
    Nakamura R, Tanino K, Miyashita M.
    Org Lett; 2005 Jul 07; 7(14):2929-32. PubMed ID: 15987172
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  • 4. Studies on the synthesis of tedanolide. 2. Stereoselective synthesis of a protected C(1)-C(12) fragment.
    Roush WR, Newcom JS.
    Org Lett; 2002 Dec 26; 4(26):4739-42. PubMed ID: 12489975
    [Abstract] [Full Text] [Related]

  • 5. Total synthesis of (+)-tedanolide.
    Smith AB, Lee D.
    J Am Chem Soc; 2007 Sep 05; 129(35):10957-62. PubMed ID: 17691787
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  • 6. Synthesis and biological properties of the cytotoxic 14-membered macrolides aspergillide A and B.
    Díaz-Oltra S, Angulo-Pachón CA, Murga J, Falomir E, Carda M, Marco JA.
    Chemistry; 2011 Jan 10; 17(2):675-88. PubMed ID: 21207589
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  • 8. Total synthesis and biological evaluation of potent analogues of dictyostatin: modification of the C2-C6 dienoate region.
    Paterson I, Gardner NM, Guzmán E, Wright AE.
    Bioorg Med Chem Lett; 2008 Dec 01; 18(23):6268-72. PubMed ID: 18951787
    [Abstract] [Full Text] [Related]

  • 9. Spiculoic acids A and B, new polyketides isolated from the Caribbean marine sponge Plakortis angulospiculatus.
    Huang XH, van Soest R, Roberge M, Andersen RJ.
    Org Lett; 2004 Jan 08; 6(1):75-8. PubMed ID: 14703354
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  • 11. Synthetic studies toward the construction of the cis-decalin portion of superstolides A and B. Application of a sequential double michael reaction and an anionic oxy-Cope rearrangement.
    Hua Z, Yu W, Su M, Jin Z.
    Org Lett; 2005 May 12; 7(10):1939-42. PubMed ID: 15876024
    [Abstract] [Full Text] [Related]

  • 12. Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 5. Stereoselective synthesis of the C13-C23 part via condensation of two fragments, C13-C17 and C18-C21, by taking advantage of the 3,4-dimethoxybenzyl protecting group.
    Zheng BZ, Maeda H, Mori M, Kusaka S, Yonemitsu O, Matsushima T, Nakajima N, Uenishi J.
    Chem Pharm Bull (Tokyo); 1999 Sep 12; 47(9):1288-96. PubMed ID: 10517009
    [Abstract] [Full Text] [Related]

  • 13. Synthesis of iriomoteolide-1a C13-C23 fragment via asymmetric conjugate addition and Julia-Kocienski coupling reaction.
    Chin YJ, Wang SY, Loh TP.
    Org Lett; 2009 Aug 20; 11(16):3674-6. PubMed ID: 19627100
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  • 15. Marine cytotoxic macrolides haterumalides and biselides, and related natural products.
    Kigoshi H, Hayakawa I.
    Chem Rec; 2007 Aug 20; 7(4):254-64. PubMed ID: 17663448
    [Abstract] [Full Text] [Related]

  • 16. An efficient and stereoselective synthesis of the monomeric counterpart of marinomycin A.
    Amans D, Bellosta V, Cossy J.
    Org Lett; 2007 Apr 12; 9(8):1453-6. PubMed ID: 17355145
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  • 18. A unified approach to the tedanolides: total synthesis of (+)-13-deoxytedanolide.
    Smith AB, Adams CM, Barbosa SA, Degnan AP.
    Proc Natl Acad Sci U S A; 2004 Aug 17; 101(33):12042-7. PubMed ID: 15163795
    [Abstract] [Full Text] [Related]

  • 19. Spirastrellolide A, an antimitotic macrolide isolated from the Caribbean marine sponge Spirastrella coccinea.
    Williams DE, Roberge M, Van Soest R, Andersen RJ.
    J Am Chem Soc; 2003 May 07; 125(18):5296-7. PubMed ID: 12720440
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