(1E,4E)-1,5-diphenyl-3-trityloxy-1,4-pentadiene | 352000-19-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: (1E,4E)-1,5-diphenyl-3-trityloxy-1,4-pentadiene
• 英文别名: [[(1E,4E)-1,5-diphenylpenta-1,4-dien-3-yl]oxy-diphenylmethyl]benzene
• CAS: 352000-19-2
• 化学式: C₃₆H₃₀O
• 分子量: 478.634
• InChiKey: GDRZCZCGYJDNDT-TUUFZWAFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.2
• 重原子数：
  37
• 可旋转键数：
  9
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (1E,4E)-1,5-diphenyl-3-trityloxy-1,4-pentadiene 在 奎宁环 、 potassium dioxotetrahydroxoosmate(VI) 、 potassium hexacyanoferrate(III) 作用下， 以 水 、 叔丁醇 为溶剂， 生成 (+/-)-(1R,2R,3S,4E)-1,5-diphenyl-3-trityloxy-4-pentene-1,2-diol 、 (+/-)-(1R,2R,3R,4E)-1,5-diphenyl-3-trityloxy-4-pentene-1,2-diol
  参考文献：
  名称：

  Substrate Binding in the Asymmetric Dihydroxylation Reaction − Investigation of the Stereoselectivity in the Dihydroxylation ofCs-Symmetric Divinylcarbinol Derivatives

  摘要：

  The mechanism of the asymmetric dihydroxylation (AD) reaction has been hotly disputed. We have studied the stereochemical outcome of the AD reaction on a series of C-s-symmetric divinylcarbinol derivatives in order to shed Light on the binding mode of the substrate to the osmium tetroxide-ligand complex. The product distribution is dependent on the size of the allylic substituent, and on the type and class of ligand. It is postulated that the diastereospecificity of the reactions originates from attractive forces between the substrate and the ligand. These interactions are independent of the interactions responsible for the enantioselectivity in the AD reaction.

  DOI：

  10.1002/1099-0690(200105)2001:9<1769::aid-ejoc1769>3.0.co;2-d
• 作为产物：
  描述：

  联甲基苯乙烯酮 在 吡啶 、 sodium tetrahydroborate 、 silver nitrate 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 146.0h， 生成 (1E,4E)-1,5-diphenyl-3-trityloxy-1,4-pentadiene
  参考文献：
  名称：

  Substrate Binding in the Asymmetric Dihydroxylation Reaction − Investigation of the Stereoselectivity in the Dihydroxylation ofCs-Symmetric Divinylcarbinol Derivatives

  摘要：

  The mechanism of the asymmetric dihydroxylation (AD) reaction has been hotly disputed. We have studied the stereochemical outcome of the AD reaction on a series of C-s-symmetric divinylcarbinol derivatives in order to shed Light on the binding mode of the substrate to the osmium tetroxide-ligand complex. The product distribution is dependent on the size of the allylic substituent, and on the type and class of ligand. It is postulated that the diastereospecificity of the reactions originates from attractive forces between the substrate and the ligand. These interactions are independent of the interactions responsible for the enantioselectivity in the AD reaction.

  DOI：

  10.1002/1099-0690(200105)2001:9<1769::aid-ejoc1769>3.0.co;2-d

文献信息

• Substrate Binding in the Asymmetric Dihydroxylation Reaction − Investigation of the Stereoselectivity in the Dihydroxylation ofCs-Symmetric Divinylcarbinol Derivatives
  作者：Annette Bayer、John S. Svendsen

  DOI：10.1002/1099-0690(200105)2001:9<1769::aid-ejoc1769>3.0.co;2-d

  日期：2001.5

  The mechanism of the asymmetric dihydroxylation (AD) reaction has been hotly disputed. We have studied the stereochemical outcome of the AD reaction on a series of C-s-symmetric divinylcarbinol derivatives in order to shed Light on the binding mode of the substrate to the osmium tetroxide-ligand complex. The product distribution is dependent on the size of the allylic substituent, and on the type and class of ligand. It is postulated that the diastereospecificity of the reactions originates from attractive forces between the substrate and the ligand. These interactions are independent of the interactions responsible for the enantioselectivity in the AD reaction.