4-methyl-1-nitro-2-prop-2-enylbenzene | 1219744-18-9

• 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: 4-methyl-1-nitro-2-prop-2-enylbenzene
• CAS: 1219744-18-9
• 化学式: C₁₀H₁₁NO₂
• 分子量: 177.203
• InChiKey: PNMYKILANPZYHL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.63
• 重原子数：
  13.0
• 可旋转键数：
  3.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  43.14
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  4-methyl-1-nitro-2-prop-2-enylbenzene 在 溶剂黄146 、 锌 作用下， 以 乙醇 为溶剂， 反应 1.0h， 生成 2-allyl-4-methyl-phenylamine
  参考文献：
  名称：

  Highly Stereoselective 7-Endo-Trig/Ring Contraction Cascade To Construct Pyrrolo[1,2-a]quinoline Derivatives

  摘要：

  With the cooperation of Cram's phenonium ion, a novel cascade reaction was illustrated to construct pyrrolo[1,2-a]quinolines as a sole diastereoisomer in good to excellent yields. Preliminary mechanistic studies revealed that the gamma-lactam ring and electron-rich arene are important driving forces for ring contraction.

  DOI：

  10.1021/ol100220c
• 作为产物：
  描述：

  3-碘-4-硝基甲苯 、 3-溴丙烯 在 苯基氯化镁 、 copper(l) cyanide 、 lithium chloride 作用下， 以 四氢呋喃 为溶剂， 生成 4-methyl-1-nitro-2-prop-2-enylbenzene
  参考文献：
  名称：

  Highly Stereoselective 7-Endo-Trig/Ring Contraction Cascade To Construct Pyrrolo[1,2-a]quinoline Derivatives

  摘要：

  With the cooperation of Cram's phenonium ion, a novel cascade reaction was illustrated to construct pyrrolo[1,2-a]quinolines as a sole diastereoisomer in good to excellent yields. Preliminary mechanistic studies revealed that the gamma-lactam ring and electron-rich arene are important driving forces for ring contraction.

  DOI：

  10.1021/ol100220c

文献信息

• Highly Stereoselective <i>7-Endo-Trig</i>/Ring Contraction Cascade To Construct Pyrrolo[1,2-<i>a</i>]quinoline Derivatives
  作者：Xinyu Li、Cheng Li、Wenjing Zhang、Xiang Lu、Shiqing Han、Ran Hong

  DOI：10.1021/ol100220c

  日期：2010.4.16

  With the cooperation of Cram's phenonium ion, a novel cascade reaction was illustrated to construct pyrrolo[1,2-a]quinolines as a sole diastereoisomer in good to excellent yields. Preliminary mechanistic studies revealed that the gamma-lactam ring and electron-rich arene are important driving forces for ring contraction.