1-Cyclopentylcyclopropane-1-carboxylic acid | 1346641-22-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 1-Cyclopentylcyclopropane-1-carboxylic acid
• 英文别名: 1-cyclopentylcyclopropane-1-carboxylic acid
• CAS: 1346641-22-2
• 化学式: C₉H₁₄O₂
• 分子量: 154.209
• InChiKey: SXTCWDQCRZCJEH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-Cyclopentylcyclopropane-1-carboxylic acid 在 草酰氯 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 12.0h， 生成 N-(4-cyano-2,3,5,6-tetrafluorophenyl)-1-cyclopentylcyclopropanecarboxamide
  参考文献：
  名称：

  Pd(II)-Catalyzed Enantioselective C–H Activation of Cyclopropanes

  摘要：

  Systematic ligand development has led to the identification of novel mono-N-protected amino acid ligands for Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. A diverse range of organoboron reagents can be used as coupling partners, and the reaction proceeds under mild conditions. These results provide a new retro-synthetic disconnection for the construction of enantioenriched cis-substituted cyclopropanecarboxylic acids.

  DOI：

  10.1021/ja207607s
• 作为产物：
  描述：

  Tert-butyl 1-cyclopentylcyclopropane-1-carboxylate 在 盐酸 、 水 作用下， 以 1,4-二氧六环 为溶剂， 生成 1-Cyclopentylcyclopropane-1-carboxylic acid
  参考文献：
  名称：

  Pd(II)-Catalyzed Enantioselective C–H Activation of Cyclopropanes

  摘要：

  Systematic ligand development has led to the identification of novel mono-N-protected amino acid ligands for Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. A diverse range of organoboron reagents can be used as coupling partners, and the reaction proceeds under mild conditions. These results provide a new retro-synthetic disconnection for the construction of enantioenriched cis-substituted cyclopropanecarboxylic acids.

  DOI：

  10.1021/ja207607s

文献信息

• Pd(II)-Catalyzed Enantioselective C–H Activation of Cyclopropanes
  作者：Masayuki Wasa、Keary M. Engle、David W. Lin、Eun Jeong Yoo、Jin-Quan Yu

  DOI：10.1021/ja207607s

  日期：2011.12.14

  Systematic ligand development has led to the identification of novel mono-N-protected amino acid ligands for Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. A diverse range of organoboron reagents can be used as coupling partners, and the reaction proceeds under mild conditions. These results provide a new retro-synthetic disconnection for the construction of enantioenriched cis-substituted cyclopropanecarboxylic acids.