ethyl (1S,2S,3S,3aR,5aS,5bS,8aS,9S,9aS,9bR)-1-(tert-butyldimethylsiloxy)-3,9-dihydroxy-9-methoxy-2,7,7-trimethyl-5-methylenedecahydro-6,8-dioxacyclopenta[b]-as-indacene-3a-carboxylate | 1003570-01-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: ethyl (1S,2S,3S,3aR,5aS,5bS,8aS,9S,9aS,9bR)-1-(tert-butyldimethylsiloxy)-3,9-dihydroxy-9-methoxy-2,7,7-trimethyl-5-methylenedecahydro-6,8-dioxacyclopenta[b]-as-indacene-3a-carboxylate
• CAS: 1003570-01-1
• 化学式: C₂₇H₄₆O₈Si
• 分子量: 526.743
• InChiKey: BCWJTSMZYRMBIP-DWPJQNGKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.61
• 重原子数：
  36.0
• 可旋转键数：
  5.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  103.68
• 氢给体数：
  2.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  ethyl (1S,2S,3S,3aR,5aS,5bS,8aS,9S,9aS,9bR)-1-(tert-butyldimethylsiloxy)-3,9-dihydroxy-9-methoxy-2,7,7-trimethyl-5-methylenedecahydro-6,8-dioxacyclopenta[b]-as-indacene-3a-carboxylate 、 三乙基硅基三氟甲磺酸酯 在 三乙胺 、 lithium aluminium tetrahydride 作用下， 以 二氯甲烷 、 四氢呋喃 为溶剂， 以9 mg的产率得到(1S,2R,3S,3aS,5aS,5bS,8aR,9aS,9bR)-1-(tert-butyldimethylsiloxy)-3a-hydroxymethyl-2,7,7-trimethyl-5-methylene-3-(triethylsiloxy)dodecahydro-6,8-dioxacyclopenta[b]-as-indacen-9-ol
  参考文献：
  名称：

  Dramatic Solvent Effect on the Diastereoselectivity of Michael Addition:  Study toward the Synthesis of the ABC Ring System of Hexacyclinic Acid

  摘要：

  During our studies toward the synthesis of the ABC ring system of hexacyclinic acid, we have observed a dramatic influence of the solvent on both our key steps. The diastereoselectivity of the intermolecular Michael addition could be totally reversed by changing the polarity of the solvent, and trifluoroethanol was found to be the optimal solvent for the following Mn(III)-promoted radical cyclization.

  DOI：

  10.1021/ol702566c
• 作为产物：
  描述：

  甲醇 、 ethyl (1S,2R,3aR,5aS,5bS,8aS,9aS,9bR)-1-(tert-butyldimethylsiloxy)-2,7,7-trimethyl-5-methylene-3,9-dioxodecahydro-6,8-dioxacyclopenta[b]-as-indacene-3a-carboxylate 在 sodium tetrahydroborate 、 cerium(III) chloride 作用下， 反应 5.0h， 以40%的产率得到ethyl (1S,2S,3S,3aR,5aS,5bS,8aS,9S,9aS,9bR)-1-(tert-butyldimethylsiloxy)-3,9-dihydroxy-9-methoxy-2,7,7-trimethyl-5-methylenedecahydro-6,8-dioxacyclopenta[b]-as-indacene-3a-carboxylate
  参考文献：
  名称：

  Dramatic Solvent Effect on the Diastereoselectivity of Michael Addition:  Study toward the Synthesis of the ABC Ring System of Hexacyclinic Acid

  摘要：

  During our studies toward the synthesis of the ABC ring system of hexacyclinic acid, we have observed a dramatic influence of the solvent on both our key steps. The diastereoselectivity of the intermolecular Michael addition could be totally reversed by changing the polarity of the solvent, and trifluoroethanol was found to be the optimal solvent for the following Mn(III)-promoted radical cyclization.

  DOI：

  10.1021/ol702566c