2-Phenylbicyclo[3.1.0]hexane-2-carboxylic acid | 156006-06-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-Phenylbicyclo[3.1.0]hexane-2-carboxylic acid
• CAS: 156006-06-3
• 化学式: C₁₃H₁₄O₂
• 分子量: 202.253
• InChiKey: JRUYXRUYVHHGES-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-Phenylbicyclo[3.1.0]hexane-2-carboxylic acid 、 2-巯基吡啶-N-氧化物 在 4-二甲氨基吡啶 、 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 以68%的产率得到(2-Sulfanylidenepyridin-1-yl) 2-phenylbicyclo[3.1.0]hexane-2-carboxylate
  参考文献：
  名称：

  Kinetic Analysis of the Rearrangement of a Conformationally Constrained .alpha.-Cyclopropylbenzyl Radical

  摘要：

  Modulation of the cyclopropylmethyl (CPM)/ homoallyl radical equilibrium by phenyl substitution at the radical center is exploited in determining the kinetic versus thermodynamic preference for bond scission in a bicyclic CPM radical. Exocyclic ring opening is determined to be 28.7 times faster than the respective endocyclic process. This method will be of general use for determining the regioselectivity of radical rearrangements.

  DOI：

  10.1021/jo00092a003
• 作为产物：
  描述：

  在 吡啶 、 4-二甲氨基吡啶 、 氢氧化钾 、 diethylzinc 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 1,4-二氧六环 、 正己烷 、 甲苯 为溶剂， 生成 2-Phenylbicyclo[3.1.0]hexane-2-carboxylic acid
  参考文献：
  名称：

  Kinetic Analysis of the Rearrangement of a Conformationally Constrained .alpha.-Cyclopropylbenzyl Radical

  摘要：

  Modulation of the cyclopropylmethyl (CPM)/ homoallyl radical equilibrium by phenyl substitution at the radical center is exploited in determining the kinetic versus thermodynamic preference for bond scission in a bicyclic CPM radical. Exocyclic ring opening is determined to be 28.7 times faster than the respective endocyclic process. This method will be of general use for determining the regioselectivity of radical rearrangements.

  DOI：

  10.1021/jo00092a003

文献信息

• Kinetic Analysis of the Rearrangement of a Conformationally Constrained .alpha.-Cyclopropylbenzyl Radical
  作者：Hariharan Venkatesan、Marc M. Greenberg

  DOI：10.1021/jo00092a003

  日期：1994.7

  Modulation of the cyclopropylmethyl (CPM)/ homoallyl radical equilibrium by phenyl substitution at the radical center is exploited in determining the kinetic versus thermodynamic preference for bond scission in a bicyclic CPM radical. Exocyclic ring opening is determined to be 28.7 times faster than the respective endocyclic process. This method will be of general use for determining the regioselectivity of radical rearrangements.