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Volumn 73, Issue 1, 2009, Pages 203-204

Isolation and absolute stereochemistry of optically active sydonic acid from Glonium sp. (Hysteriales, Ascomycota)

Author keywords

Circular dichroism (DC) spectrum; Optically active form; Sydonic acid

Indexed keywords

ACIDS; STEREOCHEMISTRY;

EID: 58949099693     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.80535     Document Type: Article
Times cited : (48)

References (9)
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    • Peng, J.1    Franzblau, S.G.2    Zhang, F.3    Hamann, M.T.4
  • 4
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    • Two new metabolites, sydonic acid and hydroxysydonic acid from Aspergillus Sydowi
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    • Hamasaki, T.1    Nagayama, K.2    Hatsuda, Y.3
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  • 6
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    • So far, we have not found any remarkable biological activity of 1.
    • So far, we have not found any remarkable biological activity of 1.
  • 7
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    • Sydonol, a new fungal morphogenic substance produced by an unidentified Aspergillus sp
    • Nukina, M., Sato, Y., Ikeda, M., and Sassa, T., Sydonol, a new fungal morphogenic substance produced by an unidentified Aspergillus sp. Agric. Biol. Chem., 45, 789-790 (1981).
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    • Nukina, M.1    Sato, Y.2    Ikeda, M.3    Sassa, T.4
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    • The solvent used for the 1H-NMR analysis was not described in ref
    • 1H-NMR analysis was not described in ref. 7.
    • , vol.7
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    • First asymmetric total synthesis of (+)-curcutetraol
    • Zhang, C., Ito, S., Hosoda, N., and Asami, M., First asymmetric total synthesis of (+)-curcutetraol. Tetrahedon Lett., 49, 2552-2554 (2008).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.