๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The structure of noranisatin, an oxidation product of anisatin

โœ Scribed by Kiyoyuki Yamada; Susumu Takada; Shiro Nakamura; Yoshimasa Hirata


Publisher
Elsevier Science
Year
1965
Tongue
French
Weight
387 KB
Volume
6
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


ABISATIN is a toxio compound obtained from the seeds of Japanese star anise* , IlliOium religiosum Sieb. et Euoc.( Illioium Aniaatum L.), --In 1952, Lane and hia oo-wrkers (1) isolated aniaatin in a pure crystalline form ( m.p. 215-22Oe, 1.1,; -27*(0 2, dioxane) ) and gave a moleoular formula, C15H2008 together with the partial atruoture shown below. 0 0 II II (CH3)2 (CllH9) (CH)5 (-C-C-C-) The moleoulsr formula by Lar group was oonfirmed in the present study: molecular weight, 328 ( mass spectrum ), C15H2008 **, m.p.


๐Ÿ“œ SIMILAR VOLUMES


Synthesis of (โˆ’)-noranisatin, an oxidati
โœ Haruki Niwa; Shigeki Ito; Takashi Hasegawa; Kazumasa Wakamatsu; Tatsuya Mori; Ki ๐Ÿ“‚ Article ๐Ÿ“… 1991 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 128 KB

The synthesis of (-)-noranisatin (2), an oxidation product of anisatin (1) possessing a novel Spiro P-lactone,was achieved starting from trio1 5 prepared from (R)-(+)-pulegone (3). Anisatin (1) is a neurotoxic sesquiterpenoid isolated from the seeds of Japanese star anise (Illicium anisurum L., shi

The structure of anisatin
โœ Kiyoyuki Yamada; Susumu Takada; Shiro Nakamura; Yoshimasa Hirata ๐Ÿ“‚ Article ๐Ÿ“… 1965 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 181 KB