(2S)-1-[(2S,5S,7R,8R)-7-[(Z,1R)-1-hydroxy-6-tri(propan-2-yl)silyloxyhex-3-enyl]-8-methyl-1,6-dioxaspiro[4.5]decan-2-yl]hept-6-en-2-ol | 936016-98-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S)-1-[(2S,5S,7R,8R)-7-[(Z,1R)-1-hydroxy-6-tri(propan-2-yl)silyloxyhex-3-enyl]-8-methyl-1,6-dioxaspiro[4.5]decan-2-yl]hept-6-en-2-ol
• CAS: 936016-98-7
• 化学式: C₃₁H₅₈O₅Si
• 分子量: 538.884
• InChiKey: FYVVZGVOLKFMOS-ARAOTPNHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.67
• 重原子数：
  37
• 可旋转键数：
  16
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  68.2
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (2S)-1-[(2S,5S,7R,8R)-7-[(Z,1R)-1-hydroxy-6-tri(propan-2-yl)silyloxyhex-3-enyl]-8-methyl-1,6-dioxaspiro[4.5]decan-2-yl]hept-6-en-2-ol 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 2.0h， 以100%的产率得到(-)-attenol A
  参考文献：
  名称：

  A Reductive Cyclization Approach to Attenol A

  摘要：

  A reductive cyclization strategy was applied to the synthesis of attenol A. This nontraditional approach to the spiroacetal structure illustrated several advantages of the reductive cyclization methodology. The attenol A core was formed in a carbon-carbon bond coupling that gave rise to a previously inaccessible spiroacetal epimer, a new method to synthesize thioketene acetals from a phenyl sulfone was realized, and the configurational stability of a nonanomeric spiroacetal was evaluated. A minor byproduct in the reductive cyclization reaction was identified that for the first time allowed direct evaluation of the stereoselectivity in a reductive cyclization of a dialkyloxy alkyllithium reagent.

  DOI：

  10.1021/jo0626459
• 作为产物：
  描述：

  but-3-ynyloxy-triisopropyl-silane 在 indium(III) chloride 、 正丁基锂 、 三乙基硼 、 二异丁基氢化铝 作用下， 以 四氢呋喃 、 乙醚 、 正己烷 为溶剂， 反应 6.5h， 生成 (2S)-1-[(2S,5S,7R,8R)-7-[(Z,1R)-1-hydroxy-6-tri(propan-2-yl)silyloxyhex-3-enyl]-8-methyl-1,6-dioxaspiro[4.5]decan-2-yl]hept-6-en-2-ol
  参考文献：
  名称：

  A Reductive Cyclization Approach to Attenol A

  摘要：

  A reductive cyclization strategy was applied to the synthesis of attenol A. This nontraditional approach to the spiroacetal structure illustrated several advantages of the reductive cyclization methodology. The attenol A core was formed in a carbon-carbon bond coupling that gave rise to a previously inaccessible spiroacetal epimer, a new method to synthesize thioketene acetals from a phenyl sulfone was realized, and the configurational stability of a nonanomeric spiroacetal was evaluated. A minor byproduct in the reductive cyclization reaction was identified that for the first time allowed direct evaluation of the stereoselectivity in a reductive cyclization of a dialkyloxy alkyllithium reagent.

  DOI：

  10.1021/jo0626459