| 191024-67-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡喃二恶英
• CAS: 191024-67-6
• 化学式: C₁₅H₁₅F₃O₄
• 分子量: 316.277
• InChiKey: VLMCOYHXGMRCFS-ZOBORPQBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.96
• 重原子数：
  22.0
• 可旋转键数：
  2.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  36.92
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  在 溶剂黄146 作用下， 生成 (2R,3S,6S)-2-(hydroxymethyl)-6-methoxy-4-(trifluoromethyl)-3,6-dihydro-2H-pyran-3-ol
  参考文献：
  名称：

  Highly stereoselective route to aldol products incorporating fluorine-containing methyl groups starting from a single d-glucose-derived intermediate

  摘要：

  Chiral aldol structures with fluorine modifications on a methyl group have been realized by utilization of the relatively rigid cyclic intermediates from the very common chiral pool compound, D-glucose, leading to attainment of the high diastereoselectivities as well as construction of differently fluorinated target materials from a single intermediate. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(97)00120-1
• 作为产物：
  描述：

  methyl 2-O-benzoyl-4,6-di-O-benzylidene-α-D-glucopyranoside 在 六甲基磷酰三胺 、 二乙胺基三氟化硫 、 Swern oxidation agent 、 二异丁基氢化铝 作用下， 生成
  参考文献：
  名称：

  Highly stereoselective route to aldol products incorporating fluorine-containing methyl groups starting from a single d-glucose-derived intermediate

  摘要：

  Chiral aldol structures with fluorine modifications on a methyl group have been realized by utilization of the relatively rigid cyclic intermediates from the very common chiral pool compound, D-glucose, leading to attainment of the high diastereoselectivities as well as construction of differently fluorinated target materials from a single intermediate. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(97)00120-1