天然有機化合物討論会講演要旨集
Online ISSN : 2433-1856
セッションID: 11
会議情報
11 アコニチン系アルカロイドにおける二・三の反応について
一戸 良行酒巻 弘細田 眞由美相見 光郎滝戸 俊夫佐藤 富次郎長谷川(山口) 槇子
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会議録・要旨集 フリー

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The absolute configuration of C_1-methoxyl group on aconitines (e.g., aconitine, mesaconitine, hypaconitine, neoline and chasmanine etc,) have been confirmed by the method of X-ray analyses. It is well known that alkaloids having allylic alcohol or ether moiety are susceptible to hydrogenolysis on some catalytic hydrogenations. On the basis of the character of metal catalyst, we reexamined the catalytic conversions of aconitine into deoxyaconitine, mesaconitine into hypaconitine (deoxymesaconitine), and jesaconitine into deoxyjesaconitine via the corresponding anhydro-type compounds. We attempted to convert delphinine into chasmanine, as we were able to isolate chasmanine and neoline from the roots of Aconitum sachalinense Fr. Schmidt.
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© 1978 天然有機化合物討論会電子化委員会
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