Syntheses of all stereoisomers of goniodiol from yeast-reduction products and their antimicrobiological activity.

نویسندگان

  • Takahiro Yoshida
  • Satoshi Yamauchi
  • Ryosuke Tago
  • Masafumi Maruyama
  • Koichi Akiyama
  • Takuya Sugahara
  • Taro Kishida
  • Yojiro Koba
چکیده

All stereoisomers of goniodiol were synthesized from yeast-reduction products. The C-6 chiral centers were converted from the chiral centers of the yeast-reduction products. Stereoselective conversion of the alkene, which had been prepared from the yeast-reduction product, to glycol constructed the C-7 and C-8 stereochemistry. (+)-Goniodiol and 7-epi-(+)-goniodiol showed the highest antibacterial activity (MIC, 3.1 mM) against Yersinia intermedia.

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عنوان ژورنال:
  • Bioscience, biotechnology, and biochemistry

دوره 72 9  شماره 

صفحات  -

تاریخ انتشار 2008