Methyl 3-phenyl-2-[(2-phenylcyclopropanecarbonyl)amino]propanoate

• 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: Methyl 3-phenyl-2-[(2-phenylcyclopropanecarbonyl)amino]propanoate
• 化学式: C₂₀H₂₁NO₃
• 分子量: 323.4
• InChiKey: BISWNYOCHHDZNZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  24
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  55.4
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• Asymmetric Cobalt-Catalyzed Cyclopropanation With Succinimidyl Diazoacetate
  申请人：Zhang X. Peter

  公开号：US20120077959A1

  公开（公告）日：2012-03-29

  Cobalt(II) complexes of the D 2 -symmetric chiral porphyrins are effective catalysts for asymmetric cyclopropanation reactions with succinimidyl diazoacetate. The Co-catalyzed reaction is suitable for various olefins, providing the corresponding cyclopropane succinimidyl esters in high yields and excellent diastereo- and enantio-selectivity. The resulting enantioenriched cyclopropane succinimidyl esters can serve as convenient synthons for the general synthesis of optically active cyclopropyl carboxamides through mild reactions with a wide range of amine derivatives, including unprotected peptides and amino sugars
• [EN] ASYMMETRIC CYCLOPROPANATION WITH SUCCINIMIDYL DIAZOACETATE<br/>[FR] CYCLOPROPANATION ASYMÉTRIQUE AVEC DU DIAZOACÉTATE DE SUCCINIMIDYLE
  申请人：UNIV SOUTH FLORIDA

  公开号：WO2010094029A2

  公开（公告）日：2010-08-19

  Cobalt(ll) complexes of the D2-symmetric chiral porphyrins are effective catalysts for asymmetric cyclopropanation reactions with succinimidyl diazoacetate. The Co-catalyzed reaction is suitable for various olefins, providing the corresponding cyclopropane succinimidyl esters in high yields and excellent diastereo- and enantio-selectivity. The resulting enantioenriched cyclopropane succinimidyl esters can serve as convenient synthons for the general synthesis of optically active cyclopropyl carboxamides through mild reactions with a wide range of amine derivatives, including unprotected peptides and amino sugars