12,22-dimethyl-3,6,9,13,17,21-hexaoxa-2,10-dioxo-14,14,20,20-tetraphenyltricyclo[17.3.0.0(11,15)]docosa-11,22-diene | 1224127-50-7

• 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: 12,22-dimethyl-3,6,9,13,17,21-hexaoxa-2,10-dioxo-14,14,20,20-tetraphenyltricyclo[17.3.0.0(11,15)]docosa-11,22-diene
• CAS: 1224127-50-7
• 化学式: C₄₂H₄₀O₈
• 分子量: 672.775
• InChiKey: VREFZOMNRFVIRG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.85
• 重原子数：
  50.0
• 可旋转键数：
  4.0
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  89.52
• 氢给体数：
  0.0
• 氢受体数：
  8.0

反应信息

• 作为产物：
  描述：

  acetoacetate diester of diethylene glycol 、 bis(3,3-diphenyl-2-propenyl) ether 在 manganese(III) triacetate dihydrate 、 溶剂黄146 作用下， 反应 0.67h， 以67%的产率得到12,22-dimethyl-3,6,9,13,17,21-hexaoxa-2,10-dioxo-14,14,20,20-tetraphenyltricyclo[17.3.0.0(11,15)]docosa-11,22-diene
  参考文献：
  名称：

  Efficient macrocyclization using methylene-tethered terminal dienes and bis(manganese(III)-enolate)s

  摘要：

  Macrocyclic compounds, which have two fused dihydrofuran rings, were synthesized with complete control by the oxidation of alpha,alpha,omega,omega-tetraaryl-alpha(omega-1)-alkadienes 1(x) with manganese(III)-oligomethylenebis(enolate) complexes directly formed by the reaction of the ohgomethylene bis(3-oxobutanoate)s 2(y) with manganese(III) acetate in situ The oxamethylene-tethered macrodiolides 5 and 7 were also produced in good to moderate yields by a similar oxidation The key intermediate, an election donor-acceptor-like complex, was proposed for the efficient macrocyclization reaction (C) 2010 Elsevier Ltd. All rights reserved

  DOI：

  10.1016/j.tet.2010.02.022