(2R,1'S)-2-[(tert-butoxycarbonylamino)(furan-2-yl)methyl]cyclohexanone | 1004750-82-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 杂芳族化合物
• 英文名称: (2R,1'S)-2-[(tert-butoxycarbonylamino)(furan-2-yl)methyl]cyclohexanone
• CAS: 1004750-82-6
• 化学式: C₁₆H₂₃NO₄
• 分子量: 293.363
• InChiKey: UHUDGVFUHJAXBH-FZMZJTMJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  21.0
• 可旋转键数：
  3.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  68.54
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  环己酮 、 (E)-tert-butyl furan-2-ylmethylenecarbamate 在 (R)-吡咯烷-3-羧酸 作用下， 以 异丙醇 为溶剂， 生成 (2R,1'S)-2-[(tert-butoxycarbonylamino)(furan-2-yl)methyl]cyclohexanone 、 、
  参考文献：
  名称：

  Catalysis of 3-Pyrrolidinecarboxylic Acid and Related Pyrrolidine Derivatives in Enantioselective anti-Mannich-Type Reactions:  Importance of the 3-Acid Group on Pyrrolidine for Stereocontrol

  摘要：

  The development of enantioselective anti-selective Mannich-type reactions of aldehydes and ketones with imines catalyzed by 3-pyrrolidinecarboxylic acid and related pyrrolidine derivatives is reported in detail. Both (3R,5R)-5-methyl-3-pyrrolidinecarboxylic acid and (R)-3-pyrrolidinecarboxylic acid efficiently catalyzed the reactions of aldehydes with alpha-imino esters under mild conditions and afforded anti-Mannich products with high diastereo- and enantioselectivities (anti/syn up to 99:1, up to >99% ee). For the reactions of ketones with a-imino esters, (R)-3-pyrrolidinecarboxylic acid was an efficient catalyst (anti/syn up to >99:1, up to 99% ee). Evaluation of a series of pyrrolidine-based catalysts indicated that the acid group at the beta-position of the pyrrolidine ring of the catalyst played an important role in forwarding the carbon-carbon bond formation and in directing anti-selectivity and enantioselectivity.

  DOI：

  10.1021/ja074907+