Rearranged Vibsane-Type Diterpenes from Viburnum awabuki and Photochemical Reaction of Vibsanin B

    • FUKUYAMA Yoshiyasu
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University
    • KUBO Miwa
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University
    • MINAMI Hiroyuki
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University
    • YUASA Hiroaki
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University

    • MATSUO Asami
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University
    • FUJII Takako
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University
    • MORISAKI Mai
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University
    • HARADA Kenichi
    • Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University

Abstract

Nine new diterpenes, neovibsanin D (1), 7-epi-neovibsanin D (2), 15-O-methylneovibsanin F (3), 14-epi-15-O-methylneovibsanin F (4), 15-O-methyl-18-oxoneovibsanin F (5), 2-O-methylneovibsanin H (6), 2-O-methylneovibsanin I (7), neovibsanin G (8), and 14-epi-neovibsanin G (9), were isolated from a methanol extract of the leaves of Viburnum awabuki. Their structures were elucidated to be uniquely rearranged vibsane-type diterpenes by spectroscopic analyses and comparison of NMR data with those of previously reported vibsane-type diterpenes. In addition, irradiation of vibsanin B (12) in methanol with a high-pressure Hg lump led to the direct formation of neovibsanins A (14) and B (15). These results gave a clue to understanding of the biogenetic interconversion of 11-membered vibsanins into neovibsanins.

Journal

Chemical & pharmaceutical bulletin   [List of Volumes]

Chemical & pharmaceutical bulletin 53(1), 72-80, 2005-01-01  [Table of Contents]

The Pharmaceutical Society of Japan

References:  17

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Codes

  • NII Article ID (NAID) :
    10016651580
  • NII NACSIS-CAT ID (NCID) :
    AA00602100
  • Text Lang :
    ENG
  • Article Type :
    ART
  • ISSN :
    00092363
  • NDL Article ID :
    7200878
  • NDL Source Classification :
    ZS51(科学技術--薬学) // ZP1(科学技術--化学・化学工業)
  • NDL Call No. :
    Z53-D167
  • Databases :
    CJP  NDL  NII-ELS  J-STAGE