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244 related items for PubMed ID: 18715038

  • 1. The unexpected isolation of CTP-431, a novel thiopyrone from the sponge Cacospongia mycofijiensis.
    Johnson TA, Amagata T, Oliver AG, Tenney K, Valeriote FA, Crews P.
    J Org Chem; 2008 Sep 19; 73(18):7255-9. PubMed ID: 18715038
    [Abstract] [Full Text] [Related]

  • 2. Origin of the Thiopyrone CTP-431 "Unexpectedly" Isolated from the Marine Sponge Cacospongia mycofijiensis.
    Przeslak AD, Inman M, Lewis W, Moody CJ.
    J Org Chem; 2018 Sep 07; 83(17):10595-10601. PubMed ID: 30044092
    [Abstract] [Full Text] [Related]

  • 3. Configuration of the psymberin amide side chain.
    Kiren S, Williams LJ.
    Org Lett; 2005 Jul 07; 7(14):2905-8. PubMed ID: 15987166
    [Abstract] [Full Text] [Related]

  • 4. Brocaenols A-C: novel polyketides from a marine derived Penicillium brocae.
    Bugni TS, Bernan VS, Greenstein M, Janso JE, Maiese WM, Mayne CL, Ireland CM.
    J Org Chem; 2003 Mar 07; 68(5):2014-7. PubMed ID: 12608826
    [Abstract] [Full Text] [Related]

  • 5. Three new spongian diterpenes from the Fijian marine sponge Spongia sp.
    Gross H, Wright AD, Reinscheid U, König GM.
    Nat Prod Commun; 2009 Mar 07; 4(3):315-22. PubMed ID: 19413106
    [Abstract] [Full Text] [Related]

  • 6. Structures of nonheme oxoiron(IV) complexes from X-ray crystallography, NMR spectroscopy, and DFT calculations.
    Klinker EJ, Kaizer J, Brennessel WW, Woodrum NL, Cramer CJ, Que L.
    Angew Chem Int Ed Engl; 2005 Jun 13; 44(24):3690-4. PubMed ID: 15915527
    [No Abstract] [Full Text] [Related]

  • 7. Spongian diterpenoids from the sponge Spongia (Heterofibria) sp.
    Ponomarenko LP, Kalinovsky AI, Afiyatullov SSh, Pushilin MA, Gerasimenko AV, Krasokhin VB, Stonik VA.
    J Nat Prod; 2007 Jul 13; 70(7):1110-3. PubMed ID: 17567172
    [Abstract] [Full Text] [Related]

  • 8. Spirastrellolides C to G: macrolides obtained from the marine sponge Spirastrella coccinea.
    Williams DE, Keyzers RA, Warabi K, Desjardine K, Riffell JL, Roberge M, Andersen RJ.
    J Org Chem; 2007 Dec 07; 72(25):9842-5. PubMed ID: 17988148
    [Abstract] [Full Text] [Related]

  • 9. First example of conformational exchange in a natural taxane enolate.
    Shi QW, Sauriol F, Park Y, Smith VH, Lord G, Zamir LO.
    Magn Reson Chem; 2005 Oct 07; 43(10):798-804. PubMed ID: 16028304
    [Abstract] [Full Text] [Related]

  • 10. The discodermolide hairpin structure flows from conformationally stable modular motifs.
    Jogalekar AS, Kriel FH, Shi Q, Cornett B, Cicero D, Snyder JP.
    J Med Chem; 2010 Jan 14; 53(1):155-65. PubMed ID: 19894728
    [Abstract] [Full Text] [Related]

  • 11. Absolute configuration of 7,8-seco-7,8-oxacassane diterpenoids from Acacia schaffneri.
    Manríquez-Torres JJ, Torres-Valencia JM, Gómez-Hurtado MA, Motilva V, García-Mauriño S, Ávila J, Talero E, Cerda-García-Rojas CM, Joseph-Nathan P.
    J Nat Prod; 2011 Sep 23; 74(9):1946-51. PubMed ID: 21894904
    [Abstract] [Full Text] [Related]

  • 12. Isolation, Structure elucidation, and antimycobacterial properties of dimeric naphtho-gamma-pyrones from the marine-derived fungus Aspergillus carbonarius.
    Zhang Y, Ling S, Fang Y, Zhu T, Gu Q, Zhu WM.
    Chem Biodivers; 2008 Jan 23; 5(1):93-100. PubMed ID: 18205129
    [Abstract] [Full Text] [Related]

  • 13. Structure revision and synthesis of a novel labdane diterpenoid from Zingiber ottensii.
    Boukouvalas J, Wang JX.
    Org Lett; 2008 Aug 21; 10(16):3397-9. PubMed ID: 18616256
    [Abstract] [Full Text] [Related]

  • 14. Correlated rotations in benzylfluorene derivatives: structure, conformation, and stereodynamics.
    Casarini D, Lunazzi L, Mazzanti A.
    J Org Chem; 2008 Apr 04; 73(7):2811-8. PubMed ID: 18327952
    [Abstract] [Full Text] [Related]

  • 15. A novel type of pentacoordinate silicon complexes and unusual ligand coupling by intramolecular electron transfer.
    Driess M, Muresan N, Merz K.
    Angew Chem Int Ed Engl; 2005 Oct 21; 44(41):6738-41. PubMed ID: 16187385
    [No Abstract] [Full Text] [Related]

  • 16. The aignopsanes, a new class of sesquiterpenes from selected chemotypes of the sponge Cacospongia mycofijiensis.
    Johnson TA, Amagata T, Sashidhara KV, Oliver AG, Tenney K, Matainaho T, Ang KK, McKerrow JH, Crews P.
    Org Lett; 2009 May 07; 11(9):1975-8. PubMed ID: 19385671
    [Abstract] [Full Text] [Related]

  • 17. Helical structure of tercyclopropanedimethanol in solution.
    Barrett AG, James RA, Morton GE, Procopiou PA, Boehme C, de Meijere A, Griesinger C, Reinscheid UM.
    J Org Chem; 2006 Mar 31; 71(7):2756-9. PubMed ID: 16555830
    [Abstract] [Full Text] [Related]

  • 18. Farnesoid X-activated receptor antagonists from a marine sponge Spongia sp.
    Nam SJ, Ko H, Shin M, Ham J, Chin J, Kim Y, Kim H, Shin K, Choi H, Kang H.
    Bioorg Med Chem Lett; 2006 Oct 15; 16(20):5398-402. PubMed ID: 16905319
    [Abstract] [Full Text] [Related]

  • 19. Tetillapyrone and nortetillapyrone, two unusual hydroxypyran-2-ones from the marine sponge Tetilla japonica.
    Watanadilok R, Sonchaeng P, Kijjoa A, Damas AM, Gales L, Silva AM, Herz W.
    J Nat Prod; 2001 Aug 15; 64(8):1056-8. PubMed ID: 11520226
    [Abstract] [Full Text] [Related]

  • 20. Determination of the absolute configuration of 6-alkylated alpha-pyrones from Ravensara crassifolia by LC-NMR.
    Queiroz EF, Wolfender JL, Raoelison G, Hostettmann K.
    Phytochem Anal; 2003 Aug 15; 14(1):34-9. PubMed ID: 12597253
    [Abstract] [Full Text] [Related]

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