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Original Articles

Isolation and Absolute Stereochemistry of Optically Active Sydonic Acid from Glonium sp. (Hysteriales, Ascomycota)

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Pages 203-204 | Received 04 Aug 2008, Accepted 09 Sep 2008, Published online: 22 May 2014

  • 1) Ono, M., Morinaga, H., Matsuoka, C., Ikeda, T., Okawa, M., Kinjo, J., and Nohara, T., New bisabolane-type sesquiterpenes from the aerial parts of Lippia dulcis. Chem. Pharm. Bull., 53, 1175–1177 (2005).
  • 2) Peng, J., Franzblau, S. G., Zhang, F., and Hamann, M. T., Novel sesquiterpenes and a lactone from the Jamaican sponge Myrmekioderma styx. Tetrahedon Lett., 43, 9699–9702 (2002).
  • 3) Mülhaupt, T., Kaspar, H., Otto, S., Reichert, M., Bringmann, G., and Lindel, T., Isolation, structural elucidation, and synthesis of curcutetraol. Eur. J. Org. Chem., 334–341 (2005).
  • 4) Hamasaki, T., Nagayama, K., and Hatsuda, Y., Two new metabolites, sydonic acid and hydroxysydonic acid from Aspergillus Sydowi. Agric. Biol. Chem., 42, 37–40 (1978).
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  • 6) So far, we have not found any remarkable biological activity of 1.
  • 7) 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).
  • 8) The solvent used for the 1H-NMR analysis was not described in ref. 7.
  • 9) 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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