(+/-)-(1S*,2S*,5S*,7R*,8R*)-1,8,9,10-Tetrachlor-5-isopropyl-11,11-dimethoxy-2-methyltricyclo<6.2.1.0^2,7>undec-9-en-3,6-dion

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: (+/-)-(1S*,2S*,5S*,7R*,8R*)-1,8,9,10-Tetrachlor-5-isopropyl-11,11-dimethoxy-2-methyltricyclo<6.2.1.0^2,7>undec-9-en-3,6-dion
• 化学式: C₁₇H₂₀Cl₄O₄
• 分子量: 430.155
• InChiKey: VKXPVJAQITXJBP-ZWJVITCESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.08
• 重原子数：
  25.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.76
• 拓扑面积：
  52.6
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  百里醌 在 溶剂黄146 、 锌 作用下， 以 四氢呋喃 为溶剂， 反应 122.5h， 生成 (+/-)-(1S*,2S*,5S*,7R*,8R*)-1,8,9,10-Tetrachlor-5-isopropyl-11,11-dimethoxy-2-methyltricyclo<6.2.1.0^2,7>undec-9-en-3,6-dion
  参考文献：
  名称：

  Versuche zur enantiomerenreinen Synthese des Chatancins, 1. Mitt. Synthese von (1R,2S,6S,7R,8S,3?S)-2-(4?-Benzyloxy-3?-methylbutoyl)-7-hydroxy-8-isopropyl-1-methylbicyclo [4.4.0]decan-4-on

  摘要：

  Our first target on the way towards the synthesis of enantiomerically pure chatancin is the preparation of the title compound. The cycloadduct of 5,5-dimethoxy- 1,2,3,4-tetrachlorocyclopentadiene and thymoquinone is stereo- and regioselectively reduced to the tricyclic ketoalcohol 4, which by nucleophilic cyclisation and reductive removal of the keto group as well as the chlorine atoms yielded a tetracyclic dimethoxyketal. Acidic hydrolysis freed the keto group, which now was treated with a chiral lithium alkyl compound derived from methyl (R)-2-methyl-3-hydroxypropionate in few steps. The resulting stereomeric tertiary alkohols were fragmented and the decalinones thus obtained separated. X-ray analysis permitted the determination of the absolute configuration of these decalinone derivatives.

  DOI：

  10.1007/bf00812715

文献信息

• Versuche zur enantiomerenreinen Synthese des Chatancins, 1. Mitt. Synthese von (1R,2S,6S,7R,8S,3?S)-2-(4?-Benzyloxy-3?-methylbutoyl)-7-hydroxy-8-isopropyl-1-methylbicyclo [4.4.0]decan-4-on
  作者：W. D. Aichberger、J. Aigner、E. G�ssinger、K. Gruber、G. Menz

  DOI：10.1007/bf00812715

  日期：——

  Our first target on the way towards the synthesis of enantiomerically pure chatancin is the preparation of the title compound. The cycloadduct of 5,5-dimethoxy- 1,2,3,4-tetrachlorocyclopentadiene and thymoquinone is stereo- and regioselectively reduced to the tricyclic ketoalcohol 4, which by nucleophilic cyclisation and reductive removal of the keto group as well as the chlorine atoms yielded a tetracyclic dimethoxyketal. Acidic hydrolysis freed the keto group, which now was treated with a chiral lithium alkyl compound derived from methyl (R)-2-methyl-3-hydroxypropionate in few steps. The resulting stereomeric tertiary alkohols were fragmented and the decalinones thus obtained separated. X-ray analysis permitted the determination of the absolute configuration of these decalinone derivatives.