JPS5920673B2 - Sesquiterpene derivatives and their production method - Google Patents

Sesquiterpene derivatives and their production method

Info

Publication number
JPS5920673B2
JPS5920673B2 JP11036078A JP11036078A JPS5920673B2 JP S5920673 B2 JPS5920673 B2 JP S5920673B2 JP 11036078 A JP11036078 A JP 11036078A JP 11036078 A JP11036078 A JP 11036078A JP S5920673 B2 JPS5920673 B2 JP S5920673B2
Authority
JP
Japan
Prior art keywords
formula
production method
sesquiterpene
sesquiterpene derivatives
mathematical
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP11036078A
Other languages
Japanese (ja)
Other versions
JPS5536442A (en
Inventor
弘幸 秋田
武 大石
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
RIKEN Institute of Physical and Chemical Research
Original Assignee
RIKEN Institute of Physical and Chemical Research
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by RIKEN Institute of Physical and Chemical Research filed Critical RIKEN Institute of Physical and Chemical Research
Priority to JP11036078A priority Critical patent/JPS5920673B2/en
Publication of JPS5536442A publication Critical patent/JPS5536442A/en
Publication of JPS5920673B2 publication Critical patent/JPS5920673B2/en
Expired legal-status Critical Current

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  • Furan Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

【発明の詳細な説明】 本発明は、式: CH3C0Oo 25H3C−0COCH3 、H 、 H3CCH3Q、 20で表わされる新規なセスキテルペン誘導体及びその
製造法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel sesquiterpene derivative represented by the formula: CH3C0Oo 25H3C-0COCH3, H, H3CCH3Q, 20, and a method for producing the same.

本発明によつて得られる上記目的化合物であるジヒドロ
キシ体13は骨格の類似している天然物のドリマン型セ
スキテルペン誘導体、例えば夜盗25蛾(Africa
narmyworm)に対する強力な摂食阻止物質作用
を示すバーバガナール(Warbur−ganal)〔
A〕、ポリゴジアール(Polygo−dial)〔別
名タデオナール( Tadeonal)〕〔B〕等へ容
易に誘導可能と考えられ、これら種30種の生理活性物
質へ変換する際の重要な中間体と考えられる。
The dihydroxy compound 13, which is the target compound obtained by the present invention, is a natural product doliman-type sesquiterpene derivative having a similar skeleton, such as the night robin moth (Africa).
Warbur-ganal is a powerful anti-feedant substance against narmyworms.
A], Polygo-dial (also known as Tadeonal) [B], etc., and is considered to be an important intermediate in the conversion to these 30 physiologically active substances.

醗力゜一。The power is one.

CH3CH3 例えば、本発明の化合物(B)からバーバガナール〔A
〕を合成する経路としては、次の工程を挙げることがで
きる。
CH3CH3 For example, from the compound (B) of the present invention to barbaganal [A
] The following steps can be mentioned as a route for synthesizing .

本願発明者らは、先にt−アビエチン酸から、コンフエ
ルテイフオリン、イソドリメニン(IsOdrimcn
in)等の他、種々のセスキテルペン化合物の合成法を
開発したが、(日本薬学会第96年会(1976年)講
演要旨集第分冊第197頁、同第97年会(1977年
)講演要旨集第分冊第197頁、特願昭52−3862
8号明細書、特開昭53−34768号公報参照)更に
t−アビエチン酸の他に広く原料を求めて、種々のセス
キテルペン誘導体の合成法について鋭意研究の結果、β
−ヨノン(1)を原料として用いることによつて、種々
のセスキテルペン誘導体を合成しうる知見を得て、本発
明を完成するに至つた。
The inventors of the present application have previously discovered that conferteiforin, isodorimenine (IsOdrimcn
In addition, he developed synthetic methods for various sesquiterpene compounds, including (197th page of Abstracts of the 96th Annual Meeting of the Pharmaceutical Society of Japan (1976), Lecture at the 97th Annual Meeting of the Pharmaceutical Society of Japan (1977)). Abstract collection, separate volume, page 197, patent application No. 52-3862
8 specification, JP-A-53-34768) Furthermore, in search of a wide range of raw materials other than t-abietic acid, as a result of intensive research on synthesis methods for various sesquiterpene derivatives, β
By using -ionone (1) as a raw material, we have obtained the knowledge that various sesquiterpene derivatives can be synthesized, and have completed the present invention.

Claims (1)

【特許請求の範囲】 1 式: ▲数式、化学式、表等があります▼ で表わされるセスキテルペン誘導体。 2 式: ▲数式、化学式、表等があります▼ で表わされる化合物を出発物質となし、これを酸化剤で
処理して式:▲数式、化学式、表等があります▼ で表わされる化合物を得ることを特徴とするセスキテル
ペン誘導体の製造法。
[Claims] 1. A sesquiterpene derivative represented by the formula: ▲There are mathematical formulas, chemical formulas, tables, etc.▼. 2 Using a compound represented by the formula: ▲Mathematical formula, chemical formula, table, etc.▼ as a starting material, and treating it with an oxidizing agent to obtain a compound represented by the formula: ▲Mathematical formula, chemical formula, table, etc.▼ A method for producing a sesquiterpene derivative characterized by:
JP11036078A 1978-09-08 1978-09-08 Sesquiterpene derivatives and their production method Expired JPS5920673B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11036078A JPS5920673B2 (en) 1978-09-08 1978-09-08 Sesquiterpene derivatives and their production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11036078A JPS5920673B2 (en) 1978-09-08 1978-09-08 Sesquiterpene derivatives and their production method

Publications (2)

Publication Number Publication Date
JPS5536442A JPS5536442A (en) 1980-03-14
JPS5920673B2 true JPS5920673B2 (en) 1984-05-15

Family

ID=14533797

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11036078A Expired JPS5920673B2 (en) 1978-09-08 1978-09-08 Sesquiterpene derivatives and their production method

Country Status (1)

Country Link
JP (1) JPS5920673B2 (en)

Also Published As

Publication number Publication date
JPS5536442A (en) 1980-03-14

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