15-(5-nitro-1H-indol-3-yl)-1,4,7,10,13-pentaoxacyclohexadecane-14,16-dione | 1006060-49-6

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酯类和类似物
• 英文名称: 15-(5-nitro-1H-indol-3-yl)-1,4,7,10,13-pentaoxacyclohexadecane-14,16-dione
• CAS: 1006060-49-6
• 化学式: C₁₉H₂₂N₂O₉
• 分子量: 422.392
• InChiKey: SOVCGBFZAULDIG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  30
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  142
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  15-diazo-1,4,7,10,13-pentaoxacyclohexadecane-14,16-dione 、 5-硝基吲哚 在 dirhodium tetraacetate 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 以61%的产率得到15-(5-nitro-1H-indol-3-yl)-1,4,7,10,13-pentaoxacyclohexadecane-14,16-dione
  参考文献：
  名称：

  Reactions of macrocyclic rhodium carbenoids: regioselective synthesis of indol-3-yl macrocyclic lactones and cryptands

  摘要：

  A wide variety of new macrocyclic diazocarbonyl compounds with various spacers was synthesized. Macrocyclic rhodium(H) carberioid insertion with various substituted indoles was performed to afford regioselectively, indol-3-yl macrocyclic di- or tetralactones (C3-alkylation). Double carberioid insertion was also performed to afford indolyl cryptand molecules. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.11.102

文献信息

• Reactions of macrocyclic rhodium carbenoids: regioselective synthesis of indol-3-yl macrocyclic lactones and cryptands
  作者：Sengodagounder Muthusamy、Boopathy Gnanaprakasam

  DOI：10.1016/j.tetlet.2007.11.102

  日期：2008.1

  A wide variety of new macrocyclic diazocarbonyl compounds with various spacers was synthesized. Macrocyclic rhodium(H) carberioid insertion with various substituted indoles was performed to afford regioselectively, indol-3-yl macrocyclic di- or tetralactones (C3-alkylation). Double carberioid insertion was also performed to afford indolyl cryptand molecules. (C) 2007 Elsevier Ltd. All rights reserved.