(3S,4R,5S,6S)-3,4-dihydroxy-5-methoxyethoxymethoxy-6-pentafluorophenyltetrahydropyran-2-one | 765941-83-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (3S,4R,5S,6S)-3,4-dihydroxy-5-methoxyethoxymethoxy-6-pentafluorophenyltetrahydropyran-2-one
• 英文别名: (3S,4R,5S,6S)-3,4-dihydroxy-5-(2-methoxyethoxymethoxy)-6-(2,3,4,5,6-pentafluorophenyl)oxan-2-one
• CAS: 765941-83-1
• 化学式: C₁₅H₁₅F₅O₇
• 分子量: 402.272
• InChiKey: OMMKFKRQLJNMLF-RFGFWPKPSA-N

物化性质

• 沸点：
  410.8±45.0 °C(predicted)
• 密度：
  1.54±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  27
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  94.4
• 氢给体数：
  2
• 氢受体数：
  12

反应信息

• 作为反应物：
  描述：

  (3S,4R,5S,6S)-3,4-dihydroxy-5-methoxyethoxymethoxy-6-pentafluorophenyltetrahydropyran-2-one 在 吡啶 、 偶氮二异丁腈 、 三正丁基氢锡 作用下， 以 二氯甲烷 、 苯 为溶剂， 生成 (4R,5S,6S)-4-hydroxy-5-(2-methoxyethoxymethoxy)-6-(2,3,4,5,6-pentafluorophenyl)oxan-2-one
  参考文献：
  名称：

  Diastereoselective Dihydroxylation and Regioselective Deoxygenation of Dihydropyranones:  A Novel Protocol for the Stereoselective Synthesis of C₁−C₈ and C₁₅−C₂₁ Subunits of (+)-Discodermolide

  摘要：

  Diastereoselective dihydroxylation of dihydropyranones and subsequent regioselective alpha-deoxygenation provides 1,3-trans-beta-hydroxy-delta-lactones stereoselectively. This protocol has been applied for the synthesis of C-1-C-8 and C-15-C-21 subunits of (+)-discodermolide.

  DOI：

  10.1021/jo0492416
• 作为产物：
  描述：

  五氟苯甲醛 在 RuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 吡啶 、 sodium hydroxide 、 四氧化锇 、 N-甲基吲哚酮 、 双氧水 作用下， 以 水 、 丙酮 、 甲苯 为溶剂， 反应 9.0h， 生成 (3S,4R,5S,6S)-3,4-dihydroxy-5-methoxyethoxymethoxy-6-pentafluorophenyltetrahydropyran-2-one
  参考文献：
  名称：

  Diastereoselective Dihydroxylation and Regioselective Deoxygenation of Dihydropyranones:  A Novel Protocol for the Stereoselective Synthesis of C₁−C₈ and C₁₅−C₂₁ Subunits of (+)-Discodermolide

  摘要：

  Diastereoselective dihydroxylation of dihydropyranones and subsequent regioselective alpha-deoxygenation provides 1,3-trans-beta-hydroxy-delta-lactones stereoselectively. This protocol has been applied for the synthesis of C-1-C-8 and C-15-C-21 subunits of (+)-discodermolide.

  DOI：

  10.1021/jo0492416

文献信息

• Diastereoselective Dihydroxylation and Regioselective Deoxygenation of Dihydropyranones:  A Novel Protocol for the Stereoselective Synthesis of C₁−C₈ and C₁₅−C₂₁ Subunits of (+)-Discodermolide
  作者：P. Veeraraghavan Ramachandran、Bodhuri Prabhudas、J. Subash Chandra、M. Venkat Ram Reddy

  DOI：10.1021/jo0492416

  日期：2004.9.1

  Diastereoselective dihydroxylation of dihydropyranones and subsequent regioselective alpha-deoxygenation provides 1,3-trans-beta-hydroxy-delta-lactones stereoselectively. This protocol has been applied for the synthesis of C-1-C-8 and C-15-C-21 subunits of (+)-discodermolide.