<2R-(2a(4R*,5R*),3aα,4α,7α,7aα)>-1-(2-methyl-1,3-dioxolan-2-yl)-5-<(octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-yl)oxy>heptan-4-ol | 135681-17-3

• 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: <2R-(2a(4R*,5R*),3aα,4α,7α,7aα)>-1-(2-methyl-1,3-dioxolan-2-yl)-5-<(octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-yl)oxy>heptan-4-ol
• 英文别名: (4R,5R)-1-(2-methyl-1,3-dioxolan-2-yl)-5-[[(1R,2S,4R,6S,7R)-1,10,10-trimethyl-3-oxatricyclo[5.2.1.02,6]decan-4-yl]oxy]heptan-4-ol
• CAS: 135681-17-3
• 化学式: C₂₃H₄₀O₅
• 分子量: 396.568
• InChiKey: PMUTVAMMILQQEX-LMCGMREZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  28
• 可旋转键数：
  8
• 环数：
  4.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  57.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  <2R-(2a(4R*,5R*),3aα,4α,7α,7aα)>-1-(2-methyl-1,3-dioxolan-2-yl)-5-<(octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-yl)oxy>heptan-4-ol 在 对甲苯磺酸 、 硫代乳酸 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 生成 (1R,7R)exo-brevicomin 、 endo-brevicomin
  参考文献：
  名称：

  Pheromone, 3.Mitt.: Eine einfache Methode zur Steuerung der Reduktion von ?-Alkoxy-carbonylverbindungen

  摘要：

  Enantiomerically pure 1,2-diols bearing optionally syn or anti configurated secondary hydroxylic groups are synthesized from acetal-protected cyanohydrins. After resolution of the diastereomers the cyanohydrins are converted into alpha-alkoxy-ketones by Grignard-reaction followed by reduction using common chelating or non-chelating agents. Among others syntheses of enantiomerically pure pheromones, endo-Brevicomin, exo-Brevicomin and Dispalure are given as examples.

  DOI：

  10.1007/bf00810831
• 作为产物：
  描述：

  [3-(2-methyl-[1,3]dioxolan-2-yl)-propyl]-magnesium chloride 以 乙醚 为溶剂， 反应 1.5h， 生成 <2R-(2a(4R*,5R*),3aα,4α,7α,7aα)>-1-(2-methyl-1,3-dioxolan-2-yl)-5-<(octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-yl)oxy>heptan-4-ol
  参考文献：
  名称：

  Pheromone, 3.Mitt.: Eine einfache Methode zur Steuerung der Reduktion von ?-Alkoxy-carbonylverbindungen

  摘要：

  Enantiomerically pure 1,2-diols bearing optionally syn or anti configurated secondary hydroxylic groups are synthesized from acetal-protected cyanohydrins. After resolution of the diastereomers the cyanohydrins are converted into alpha-alkoxy-ketones by Grignard-reaction followed by reduction using common chelating or non-chelating agents. Among others syntheses of enantiomerically pure pheromones, endo-Brevicomin, exo-Brevicomin and Dispalure are given as examples.

  DOI：

  10.1007/bf00810831

文献信息

• ——
  作者：NOE C. R.、 KNOLLMULLER M.

  DOI：——

  日期：——
• Pheromone, 3.Mitt.: Eine einfache Methode zur Steuerung der Reduktion von ?-Alkoxy-carbonylverbindungen
  作者：Christian R. Noe、M. Knollm�ller、G. Steinbauer、E. Wagner、H. K�rner、P. Ettmayer、H. V�llenkle

  DOI：10.1007/bf00810831

  日期：1991.4

  Enantiomerically pure 1,2-diols bearing optionally syn or anti configurated secondary hydroxylic groups are synthesized from acetal-protected cyanohydrins. After resolution of the diastereomers the cyanohydrins are converted into alpha-alkoxy-ketones by Grignard-reaction followed by reduction using common chelating or non-chelating agents. Among others syntheses of enantiomerically pure pheromones, endo-Brevicomin, exo-Brevicomin and Dispalure are given as examples.