(5S,6S)-5,6-(isopropylidenedioxy)-8-phenyloct-1-en-7-yne | 249603-83-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (5S,6S)-5,6-(isopropylidenedioxy)-8-phenyloct-1-en-7-yne
• 英文别名: (4S,5S)-4-but-3-enyl-2,2-dimethyl-5-(2-phenylethynyl)-1,3-dioxolane
• CAS: 249603-83-6
• 化学式: C₁₇H₂₀O₂
• 分子量: 256.345
• InChiKey: IIZINMCZVTYWQT-HOTGVXAUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  19
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (5S,6S)-5,6-(isopropylidenedioxy)-8-phenyloct-1-en-7-yne 在 对甲苯磺酸 作用下， 以 甲醇 为溶剂， 反应 24.0h， 以95%的产率得到(3S,4S)-1-phenyloct-7-en-1-yne-3,4-diol
  参考文献：
  名称：

  Stereocomplementary Construction of Optically Active Bicyclo[4.3.0]nonenone Derivatives

  摘要：

  Treatment of (5S,6S)-5,6-bis(tert-butyldimethylsiloxy)-8-(substituted)oct-1-en-7-yne derivatives, prepared from diethyl L-tartrate, with Co-2(CO)(8) afforded the corresponding cobalt-complexed enynes, which were subsequently exposed to the typical Pauson-Khand conditions to furnish highly stereoselectively or exclusively (2S,3S,6S)-2,3-bis(tert-butyldimetbylsiloxy)-9-(substituted)bicyclo[4.3.0]non-1(9)-en-8-ones. On the other hand, (3S,4S)-1-(substituted)oct-7-en-1-yne-3,4-diol congeners produced, on exposure to the Pauson-Khand conditions, (2S,3S,6R)-2,3-dihydroxy-9-(substituted) bicyclo[4.3.0]-non-1(9)-en-8-one derivatives in a highly stereoselective manner. The newly developed procedure has been shown to be useful for construction of the 2,3-bis(oxygenated)-7-(substituted)-bicyclo[4.3.0]non-6-en-8-one framework in a stereocomplementary as well as stereoselective fashion.

  DOI：

  10.1021/jo990819z
• 作为产物：
  描述：

  (2R,3R)-2,3-isopropylidendioxy-6-hepten-1-ol 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 、 正丁基锂 、 草酰氯 、 二甲基亚砜 、 三乙胺 、 二异丙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 乙醚 、 正己烷 、 二氯甲烷 为溶剂， 反应 4.67h， 生成 (5S,6S)-5,6-(isopropylidenedioxy)-8-phenyloct-1-en-7-yne
  参考文献：
  名称：

  Stereocomplementary Construction of Optically Active Bicyclo[4.3.0]nonenone Derivatives

  摘要：

  Treatment of (5S,6S)-5,6-bis(tert-butyldimethylsiloxy)-8-(substituted)oct-1-en-7-yne derivatives, prepared from diethyl L-tartrate, with Co-2(CO)(8) afforded the corresponding cobalt-complexed enynes, which were subsequently exposed to the typical Pauson-Khand conditions to furnish highly stereoselectively or exclusively (2S,3S,6S)-2,3-bis(tert-butyldimetbylsiloxy)-9-(substituted)bicyclo[4.3.0]non-1(9)-en-8-ones. On the other hand, (3S,4S)-1-(substituted)oct-7-en-1-yne-3,4-diol congeners produced, on exposure to the Pauson-Khand conditions, (2S,3S,6R)-2,3-dihydroxy-9-(substituted) bicyclo[4.3.0]-non-1(9)-en-8-one derivatives in a highly stereoselective manner. The newly developed procedure has been shown to be useful for construction of the 2,3-bis(oxygenated)-7-(substituted)-bicyclo[4.3.0]non-6-en-8-one framework in a stereocomplementary as well as stereoselective fashion.

  DOI：

  10.1021/jo990819z

文献信息

• Stereocomplementary Construction of Optically Active Bicyclo[4.3.0]nonenone Derivatives
  作者：Chisato Mukai、Jin Sung Kim、Hiroshi Sonobe、Miyoji Hanaoka

  DOI：10.1021/jo990819z

  日期：1999.9.1

  Treatment of (5S,6S)-5,6-bis(tert-butyldimethylsiloxy)-8-(substituted)oct-1-en-7-yne derivatives, prepared from diethyl L-tartrate, with Co-2(CO)(8) afforded the corresponding cobalt-complexed enynes, which were subsequently exposed to the typical Pauson-Khand conditions to furnish highly stereoselectively or exclusively (2S,3S,6S)-2,3-bis(tert-butyldimetbylsiloxy)-9-(substituted)bicyclo[4.3.0]non-1(9)-en-8-ones. On the other hand, (3S,4S)-1-(substituted)oct-7-en-1-yne-3,4-diol congeners produced, on exposure to the Pauson-Khand conditions, (2S,3S,6R)-2,3-dihydroxy-9-(substituted) bicyclo[4.3.0]-non-1(9)-en-8-one derivatives in a highly stereoselective manner. The newly developed procedure has been shown to be useful for construction of the 2,3-bis(oxygenated)-7-(substituted)-bicyclo[4.3.0]non-6-en-8-one framework in a stereocomplementary as well as stereoselective fashion.