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Journal Abstract Search

135 related items for PubMed ID: 12509899

  • 21. Absolute stereochemistry of amphidinolide Q.
    Takahashi Y, Kubota T, Fukushi E, Kawabata J, Kobayashi J.
    Org Lett; 2008 Sep 04; 10(17):3709-11. PubMed ID: 18680307
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  • 22. Automatic assignment of absolute configuration from 1D NMR data.
    Zhang QY, Carrera G, Gomes MJ, Aires-de-Sousa J.
    J Org Chem; 2005 Mar 18; 70(6):2120-30. PubMed ID: 15760195
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  • 23. 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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  • 27. Use of a chiral praseodymium shift reagent in predicting the complete stereostructure of glisoprenin A.
    Ghosh I, Kishi Y, Tomoda H, Omura S.
    Org Lett; 2004 Dec 09; 6(25):4719-22. PubMed ID: 15575669
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  • 28. An enantioselective NMR shift reagent for cationic aromatics.
    Dignam CF, Richards CJ, Zopf JJ, Wacker LS, Wenzel TJ.
    Org Lett; 2005 Apr 28; 7(9):1773-6. PubMed ID: 15844903
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  • 30. Absolute stereochemistry of immunosuppressive macrolide brasilinolide A and its new congener brasilinolide C.
    Komatsu K, Tsuda M, Tanaka Y, Mikami Y, Kobayashi J.
    J Org Chem; 2004 Mar 05; 69(5):1535-41. PubMed ID: 14987008
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  • 31. Macrolactin N, a new peptide deformylase inhibitor produced by Bacillus subtilis.
    Yoo JS, Zheng CJ, Lee S, Kwak JH, Kim WG.
    Bioorg Med Chem Lett; 2006 Sep 15; 16(18):4889-92. PubMed ID: 16809037
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  • 36. Toward the creation of NMR databases in chiral solvents: bidentate chiral NMR solvents for assignment of the absolute configuration of acyclic secondary alcohols.
    Kobayashi Y, Hayashi N, Kishi Y.
    Org Lett; 2002 Feb 07; 4(3):411-4. PubMed ID: 11820892
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  • 39. Molecular insights into 14-membered macrolides using the MM-PBSA method.
    Yam WK, Wahab HA.
    J Chem Inf Model; 2009 Jun 07; 49(6):1558-67. PubMed ID: 19469526
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