Planta Med 2001; 67(5): 480-481
DOI: 10.1055/s-2001-15812
Letter

© Georg Thieme Verlag Stuttgart · New York

Absolute Configuration of (6S,9S)-Roseoside from Polygonum hydropiper

Yoshihiro Murai1,*, Shigenori Kashimura1 , Syouhei Tamezawa1 , Toshihiro Hashimoto2 , Shigeru Takaoka2 , Yoshinori Asakawa2 , Kazuo Kiguchi3 , Fujio Murai4 , Motoko Tagawa4
  • 1 Faculty of Science and Technology, Kinki University, Osaka, Japan
  • 2 Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Tokushima, Japan
  • 3 Japan Sangaria Co. Ltd., Osaka, Japan
  • 4 Laboratory of Chemistry, Aichi Medical University, Aichi, Japan
Further Information

Publication History

July 27, 2000

October 29, 2000

Publication Date:
31 December 2001 (online)

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Abstract

From Polygonum hydropiper L., a C13-norisoprenoid glucoside was isolated and its absolute configuration was established to be (6S,9S)-roseoside (1) by spectroscopic evidence and X-ray crystallographic analysis of its acetate derivative (2). In addition, the stereostructure of roseoside from Canthium subcordatum was revised to the (6S,9S) configuration.

References

Dr. Yoshihiro Murai

Faculty of Science and Technology

Kinki University

3-4-1 Kowakae

Higashi-Osaka

Osaka 577-8502

Japan

Email: murai@meta.kindai.ac.jp

Fax: +81-66723-2721