methyl 6-oxo-5-phenylbenzo[c]phenanthridine-12-carboxylate | 128637-89-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: methyl 6-oxo-5-phenylbenzo[c]phenanthridine-12-carboxylate
• CAS: 128637-89-8
• 化学式: C₂₅H₁₇NO₃
• 分子量: 379.415
• InChiKey: VZVFHYVOXDDJTP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.08
• 重原子数：
  29.0
• 可旋转键数：
  2.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.04
• 拓扑面积：
  48.3
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  邻氨基苯甲酸 、 methyl 5,6-dihydro-3,6-dioxo-5-phenyl-3H-pyrano<2,3-c>isoquinoline-2-carboxylate 在 亚硝酸异戊酯 作用下， 生成 methyl 6-oxo-5-phenylbenzo[c]phenanthridine-12-carboxylate
  参考文献：
  名称：

  A new approach to the synthesis of antitumor benzophenanthridine alkaloids. Formal synthesis of nitidine

  摘要：

  The synthesis of benzophenanthridine alkaloids by an efficient new convergent strategy based on the Diels-Alder reaction between an alpha-pyrone and an aryne is described. With minor modifications, norbenzophenanthridines and phenanthridines and their 12-amino derivatives were obtained in good overall yields.

  DOI：

  10.1021/jo00048a025

文献信息

• A new intermolecular benzyne cycloaddition approach to benzophenanthridines
  作者：D.Pérez Meirás、E. Guitián、L. Castedo

  DOI：10.1016/s0040-4039(00)94356-9

  日期：——

  The Intermolecular Benzyne Cycloaddition (IBC) approach was used for the synthesis of benzophenanthridines by constructing ring C in the key cycloaddition step

  在关键的环加成步骤中，通过环C的构建，使用分子间苯并环加成法（IBC）合成苯并菲啶
• MEIRAS, D. PEREZ;GUITIAN, E.;CASTEDO, L., TETRAHEDRON LETT., 31,(1990) N, C. 143-144
  作者：MEIRAS, D. PEREZ、GUITIAN, E.、CASTEDO, L.

  DOI：——

  日期：——
• A new approach to the synthesis of antitumor benzophenanthridine alkaloids. Formal synthesis of nitidine
  作者：Dolores Perez、Enrique Guitian、Luis Castedo

  DOI：10.1021/jo00048a025

  日期：1992.10

  The synthesis of benzophenanthridine alkaloids by an efficient new convergent strategy based on the Diels-Alder reaction between an alpha-pyrone and an aryne is described. With minor modifications, norbenzophenanthridines and phenanthridines and their 12-amino derivatives were obtained in good overall yields.