5,5,5',5'-tetramethoxyl-6,6'-di(2-naphthalenyl)-1,1'-bi(cyclohex-3-ene)-2,2'-dione | 1260433-74-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 5,5,5',5'-tetramethoxyl-6,6'-di(2-naphthalenyl)-1,1'-bi(cyclohex-3-ene)-2,2'-dione
• CAS: 1260433-74-6
• 化学式: C₃₆H₃₄O₆
• 分子量: 562.662
• InChiKey: BVYZLKNWULBRNT-CUPIEXAXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.35
• 重原子数：
  42.0
• 可旋转键数：
  7.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  71.06
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  5,5,5',5'-tetramethoxyl-6,6'-di(2-naphthalenyl)-1,1'-bi(cyclohex-3-ene)-2,2'-dione 在 三氟化硼乙醚 作用下， 以 甲苯 为溶剂， 以82%的产率得到(S)-5,5'-dimethoxy-6,6'-di(2-naphthalenyl)biphenyl-2,2'-diol
  参考文献：
  名称：

  Enantioselective Synthesis of Biphenols from 1,4-Diketones by Traceless Central-to-Axial Chirality Exchange

  摘要：

  A method for the enantioselective synthesis of biphenols from readily prepared 1,4-diketones is reported. Key to the success of this method is the highly selective transfer of central to axial chirality during a double aromatization event triggered by BF3 center dot OEt2. On the basis of X-ray crystallographic data, a stereochemical model for this chirality exchange process is put forth.

  DOI：

  10.1021/ja108717r
• 作为产物：
  描述：

  4,4-dimethoxy-5-(2-naphthalenyl)-2-cyclohexenone 在 lithium diisopropyl amide 、 copper dichloride 作用下， 以 四氢呋喃 为溶剂， 反应 0.5h， 以51%的产率得到5,5,5',5'-tetramethoxyl-6,6'-di(2-naphthalenyl)-1,1'-bi(cyclohex-3-ene)-2,2'-dione
  参考文献：
  名称：

  Enantioselective Synthesis of Biphenols from 1,4-Diketones by Traceless Central-to-Axial Chirality Exchange

  摘要：

  A method for the enantioselective synthesis of biphenols from readily prepared 1,4-diketones is reported. Key to the success of this method is the highly selective transfer of central to axial chirality during a double aromatization event triggered by BF3 center dot OEt2. On the basis of X-ray crystallographic data, a stereochemical model for this chirality exchange process is put forth.

  DOI：

  10.1021/ja108717r