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Journal Abstract Search

78 related items for PubMed ID: 11456839

  • 1. 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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  • 2. 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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  • 3. 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. Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Proof.
    Tan CH, Kobayashi Y, Kishi Y.
    Angew Chem Int Ed Engl; 2000 Dec 01; 39(23):4282-4284. PubMed ID: 29711890
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  • 5. Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Prediction.
    Kobayashi Y, Tan CH, Kishi Y.
    Angew Chem Int Ed Engl; 2000 Dec 01; 39(23):4279-4281. PubMed ID: 29711895
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  • 13. Structure determination of the antibiotic desertomycin B by fast-atom bombardment mass spectrometric techniques.
    Dinya Z, Sztaricskai F, Horváth G.
    Rapid Commun Mass Spectrom; 1991 Nov 01; 5(11):534-7. PubMed ID: 1756288
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  • 15. Structures of new 18-membered macrolides FD-891 and FD-892.
    Seki-Asano M, Tsuchida Y, Hanada K, Mizoue K.
    J Antibiot (Tokyo); 1994 Nov 01; 47(11):1234-41. PubMed ID: 8002385
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  • 16. The stereochemical outcome of electrophilic addition reactions on the 5,6-double bond in the spinosyns.
    De Amicis CV, Graupner PR, Erickson JA, Paschal JW, Kirst HA, Creemer LC, Fanwick PE.
    J Org Chem; 2001 Dec 14; 66(25):8431-5. PubMed ID: 11735521
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  • 20. Toward the synthesis of the antibiotic branimycin: novel approaches to highly substituted cis-decalin systems.
    Mulzer J, Castagnolo D, Felzmann W, Marchart S, Pilger C, Enev VS.
    Chemistry; 2006 Aug 07; 12(23):5992-6001. PubMed ID: 16710867
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