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Journal Abstract Search

135 related items for PubMed ID: 12509899

  • 1. Complete stereochemistry of tetrafibricin.
    Kobayashi Y, Czechtizky W, Kishi Y.
    Org Lett; 2003 Jan 09; 5(1):93-6. PubMed ID: 12509899
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  • 2. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: scope and limitation.
    Hayashi N, Kobayashi Y, Kishi Y.
    Org Lett; 2001 Jul 12; 3(14):2249-52. PubMed ID: 11440591
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  • 4. Determination of the three-dimensional, solution-phase structure of the macrolide antibiotic oxolide in CD2Cl2 and D2O from NMR constraints.
    Steinmetz WE, Sparrow A, Somsouk M.
    Magn Reson Chem; 2005 Jan 12; 43(1):16-20. PubMed ID: 15468276
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  • 5. Divergolides A-D from a mangrove endophyte reveal an unparalleled plasticity in ansa-macrolide biosynthesis.
    Ding L, Maier A, Fiebig HH, Görls H, Lin WH, Peschel G, Hertweck C.
    Angew Chem Int Ed Engl; 2011 Feb 11; 50(7):1630-4. PubMed ID: 21308920
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  • 7. Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: proof of concept.
    Lee J, Kobayashi Y, Tezuka K, Kishi Y.
    Org Lett; 1999 Dec 30; 1(13):2181-4. PubMed ID: 10836073
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  • 8. Systematic approach to understanding macrolide-ribosome interactions: NMR and modeling studies of oleandomycin and its derivatives.
    Novak P, Tatić I, Tepes P, Kostrun S, Barber J.
    J Phys Chem A; 2006 Jan 19; 110(2):572-9. PubMed ID: 16405329
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  • 12. Toward creation of a universal NMR database for stereochemical assignment: complete structure of the desertomycin/oasomycin class of natural products.
    Kobayashi Y, Tan CH, Kishi Y.
    J Am Chem Soc; 2001 Mar 07; 123(9):2076-8. PubMed ID: 11456839
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  • 14. Stereostructure of a novel cytotoxic 18-membered macrolactone antibiotic FD-891.
    Eguchi T, Kobayashi K, Uekusa H, Ohashi Y, Mizoue K, Matsushima Y, Kakinuma K.
    Org Lett; 2002 Oct 03; 4(20):3383-6. PubMed ID: 12323024
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  • 15. Structure of subtilosin A, a cyclic antimicrobial peptide from Bacillus subtilis with unusual sulfur to alpha-carbon cross-links: formation and reduction of alpha-thio-alpha-amino acid derivatives.
    Kawulka KE, Sprules T, Diaper CM, Whittal RM, McKay RT, Mercier P, Zuber P, Vederas JC.
    Biochemistry; 2004 Mar 30; 43(12):3385-95. PubMed ID: 15035610
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  • 16. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: NMR desymmetrization of meso compounds.
    Kobayashi Y, Hayashi N, Kishi Y.
    Org Lett; 2001 Jul 12; 3(14):2253-5. PubMed ID: 11440592
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  • 18. Chiral shift reagent for amino acids based on resonance-assisted hydrogen bonding.
    Chin J, Kim DC, Kim HJ, Panosyan FB, Kim KM.
    Org Lett; 2004 Jul 22; 6(15):2591-3. PubMed ID: 15255698
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  • 19. Determination of the enantiomeric composition of chiral delta-2-oxazolines-1,3 by 1H and 19F NMR spectroscopy using chiral solvating agents.
    Beaufour M, Merelli B, Menguy L, Cherton JC.
    Chirality; 2003 May 15; 15(5):382-90. PubMed ID: 12692883
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  • 20. Application of residual dipolar couplings in organic compounds.
    Yan J, Zartler ER.
    Magn Reson Chem; 2005 Jan 15; 43(1):53-64. PubMed ID: 15578593
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