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Synthesis of 3-Oxosapriparaquinone, a Diterpene fromSalvia prionitisHance
Bulletin of the Chemical Society of Japan ( IF 3.3 ) Pub Date : 1995-09-01 , DOI: 10.1246/bcsj.68.2705 Takashi Matsumoto 1 , Yoshio Takeda 1 , Kimiko Soh 1 , Hiroyuki Matsumura 1 , Sachihiko Imai 2
Bulletin of the Chemical Society of Japan ( IF 3.3 ) Pub Date : 1995-09-01 , DOI: 10.1246/bcsj.68.2705 Takashi Matsumoto 1 , Yoshio Takeda 1 , Kimiko Soh 1 , Hiroyuki Matsumura 1 , Sachihiko Imai 2
Affiliation
12-Acetoxy-5,10-friedo-4,5-seco-abieta-3,5(10),6,8,11,13-hexaene prepared from (+)-dehydroabietic acid, was converted into a natural rearranged abietane-type diterpene, 3-oxosapriparaquinone, via 12-benzoyloxy-3-hydroxy-5,10-friedo-4,5-seco-abieta-5(10),6,8,12-tetraene-11,14-dione by a series of reactions: hydroboration–oxidation, benzoyl peroxide oxidation, Jones oxidation, and alkaline hydrolysis.
中文翻译:
3-Oxosapriparaquinone 的合成,一种来自丹参的二萜
12-Acetoxy-5,10-friedo-4,5-seco-abieta-3,5(10),6,8,11,13-己烯由(+)-脱氢松香酸制备,转化为天然重排松香烷-型二萜, 3-oxosapriparaquinone, via 12-benzoyloxy-3-hydroxy-5,10-friedo-4,5-seco-abieta-5(10),6,8,12-tetraene-11,14-dione一系列反应:硼氢化-氧化、过氧化苯甲酰氧化、琼斯氧化和碱水解。
更新日期:1995-09-01
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
3-Oxosapriparaquinone 的合成,一种来自丹参的二萜
12-Acetoxy-5,10-friedo-4,5-seco-abieta-3,5(10),6,8,11,13-己烯由(+)-脱氢松香酸制备,转化为天然重排松香烷-型二萜, 3-oxosapriparaquinone, via 12-benzoyloxy-3-hydroxy-5,10-friedo-4,5-seco-abieta-5(10),6,8,12-tetraene-11,14-dione一系列反应:硼氢化-氧化、过氧化苯甲酰氧化、琼斯氧化和碱水解。