7-hydroxy-2,3-(2',3'-quinolino)tetracyclo<6.3.0.0^4,11.0^5,9>undecane | 131251-63-3

• 分子结构分类: 有机化合物 - 生物碱及其衍生物
• 英文名称: 7-hydroxy-2,3-(2',3'-quinolino)tetracyclo<6.3.0.0^4,11.0^5,9>undecane
• CAS: 131251-63-3
• 化学式: C₁₈H₁₇NO
• 分子量: 263.339
• InChiKey: NUARYEUDCSTYAN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.06
• 重原子数：
  20.0
• 可旋转键数：
  0.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  33.12
• 氢给体数：
  1.0
• 氢受体数：
  2.0

反应信息

• 作为产物：
  描述：

  7,6-(2',3'-quinolino)tetracyclo<6.3.0.0^4,11.0^5,9>undecane-2-one 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 反应 16.0h， 以80%的产率得到7-hydroxy-2,3-(2',3'-quinolino)tetracyclo<6.3.0.0^4,11.0^5,9>undecane
  参考文献：
  名称：

  Heteroaromatic fused derivatives of tetracyclo[6.3.0.04,11.O5,9]undecane

  摘要：

  A series of rigid syn-orthocyclophanes is prepared by the Friedlander condensation of appropriate o-amino-benzaldehyde derivatives with tetracyclo[6.3.0.0(4,11).0(5,9)]undecane-2,7-dione. The reaction may proceed in a stepwise fashion so that unsymmetrical layered compounds can be prepared. These species can be further elaborated by oxidation to quinolinequinones or N-oxides and quaternization to quinolinium salts. Molecular mechanics calculations agree closely with X-ray analysis in describing the structural properties of these cyclophanes. Analysis of the H-1 NMR and UV spectra as well as the reduction potentials of these molecules support a moderate electronic interaction between the decks. Initial investigations regarding their ability to serve as cleft-type hosts are described.

  DOI：

  10.1021/jo00004a029