38-Oxa-8,17,22,31-tetrazaoctacyclo[31.3.1.12,6.13,36.07,15.09,14.024,32.025,30]nonatriaconta-1(36),2,4,6(39),7(15),9,11,13,24(32),25,27,29,33(37),34-tetradecaene | 1402073-91-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并呋喃
• 英文名称: 38-Oxa-8,17,22,31-tetrazaoctacyclo[31.3.1.12,6.13,36.07,15.09,14.024,32.025,30]nonatriaconta-1(36),2,4,6(39),7(15),9,11,13,24(32),25,27,29,33(37),34-tetradecaene
• 英文别名: 38-oxa-8,17,22,31-tetrazaoctacyclo[31.3.1.12,6.13,36.07,15.09,14.024,32.025,30]nonatriaconta-1(36),2,4,6(39),7(15),9,11,13,24(32),25,27,29,33(37),34-tetradecaene
• CAS: 1402073-91-9
• 化学式: C₃₄H₃₀N₄O
• 分子量: 510.638
• InChiKey: KPJGWJQHJXPXDE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  39
• 可旋转键数：
  0
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  68.8
• 氢给体数：
  4
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2,2'-(dibenzo[b,d]furan-2,8-diyl)bis(1H-indole-3-carbaldehyde) 在 sodium tetrahydroborate 作用下， 以 乙醇 为溶剂， 反应 12.0h， 生成 38-Oxa-8,17,22,31-tetrazaoctacyclo[31.3.1.12,6.13,36.07,15.09,14.024,32.025,30]nonatriaconta-1(36),2,4,6(39),7(15),9,11,13,24(32),25,27,29,33(37),34-tetradecaene
  参考文献：
  名称：

  Synthesis of macrocyclic systems derived from di-(2-indolyl)heteroarenes

  摘要：

  A number of new 3,6-di-(2-indolyl)-dibenzofuran and carbazole derivatives have been prepared from dibenzofuran and carbazole linkers via the Fischer indole synthesis. The bis-indoles were successfully formylated at C3 and the resulting dicarbaldehydes were combined with diamines to generate indole based imine macrocyclic systems. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2012.08.063

文献信息

• Synthesis of macrocyclic systems derived from di-(2-indolyl)heteroarenes
  作者：Ibrahim F. Sengul、Kasey Wood、Naresh Kumar、David StC. Black

  DOI：10.1016/j.tet.2012.08.063

  日期：2012.11

  A number of new 3,6-di-(2-indolyl)-dibenzofuran and carbazole derivatives have been prepared from dibenzofuran and carbazole linkers via the Fischer indole synthesis. The bis-indoles were successfully formylated at C3 and the resulting dicarbaldehydes were combined with diamines to generate indole based imine macrocyclic systems. (C) 2012 Elsevier Ltd. All rights reserved.