(Z)-1-acetyloxy-1,3,3-triphenyl-1-propene | 148868-89-7

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: (Z)-1-acetyloxy-1,3,3-triphenyl-1-propene
• CAS: 148868-89-7
• 化学式: C₂₃H₂₀O₂
• 分子量: 328.411
• InChiKey: AGHZEEKOVZZKMH-QJOMJCCJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.42
• 重原子数：
  25.0
• 可旋转键数：
  5.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  26.3
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  (Z)-1-acetyloxy-1,3,3-triphenyl-1-propene 在 三氯化铝 、 溴 作用下， 以 四氯化碳 、 正己烷 为溶剂， 反应 2.0h， 生成 2-溴-1,3,3-三苯基-1-丙酮
  参考文献：
  名称：

  Direct photolysis and electron transfer photooxygenation of enol acetates of 3-phenylpropiophenones

  摘要：

  Direct photolysis of enol acetates of 3-phenylpropiophenones la-c gives rise to the parent propiophenones 2a-c and the 1,3-acyl shift products 3a-c. By contrast, 2,4,6-triphenylpyrylium tetrafluoroborate sensitized photolysis of substrates la-c affords the alpha-acetyloxypropiophenones 79-c as the most general products. These results have been rationalized according to the generation of radical pairs in the direct photolysis and radical cations in the photoinduced electron transfer processes.

  DOI：

  10.1007/bf00808680
• 作为产物：
  描述：

  乙酸异丙烯酯 、 1,3,3-三苯基-1-丙酮 在 对甲苯磺酸 作用下， 以65%的产率得到(Z)-1-acetyloxy-1,3,3-triphenyl-1-propene
  参考文献：
  名称：

  Direct photolysis and electron transfer photooxygenation of enol acetates of 3-phenylpropiophenones

  摘要：

  Direct photolysis of enol acetates of 3-phenylpropiophenones la-c gives rise to the parent propiophenones 2a-c and the 1,3-acyl shift products 3a-c. By contrast, 2,4,6-triphenylpyrylium tetrafluoroborate sensitized photolysis of substrates la-c affords the alpha-acetyloxypropiophenones 79-c as the most general products. These results have been rationalized according to the generation of radical pairs in the direct photolysis and radical cations in the photoinduced electron transfer processes.

  DOI：

  10.1007/bf00808680

文献信息

• Direct photolysis and electron transfer photooxygenation of enol acetates of 3-phenylpropiophenones
  作者：Felipe Algarra、Mar�a V. Baldov�、Hermenegildo Garc�a、Miguel A. Miranda、Jaime Primo

  DOI：10.1007/bf00808680

  日期：1993.2

  Direct photolysis of enol acetates of 3-phenylpropiophenones la-c gives rise to the parent propiophenones 2a-c and the 1,3-acyl shift products 3a-c. By contrast, 2,4,6-triphenylpyrylium tetrafluoroborate sensitized photolysis of substrates la-c affords the alpha-acetyloxypropiophenones 79-c as the most general products. These results have been rationalized according to the generation of radical pairs in the direct photolysis and radical cations in the photoinduced electron transfer processes.