(2R,3S,3aR)-tert-butyl 3-(4-methoxyphenyl)-2,3,3a,4-tetrahydrochromeno[4,3-b]pyrrole-2-carboxylate | 1373520-27-4

• 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: (2R,3S,3aR)-tert-butyl 3-(4-methoxyphenyl)-2,3,3a,4-tetrahydrochromeno[4,3-b]pyrrole-2-carboxylate
• 英文别名: tert-butyl (2R,3S,3aR)-3-(4-methoxyphenyl)-2,3,3a,4-tetrahydrochromeno[4,3-b]pyrrole-2-carboxylate
• CAS: 1373520-27-4
• 化学式: C₂₃H₂₅NO₄
• 分子量: 379.456
• InChiKey: IUXBUEFZDBIFII-YFVAEKQCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  28
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  57.1
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  (E)-3-(4-methoxybenzylidene)chroman-4-one 、 N-二苯亚甲基-甘氨酸叔丁酯 在 C₇₀H₄₀F₂₄NO⁽¹⁺⁾*Br^(1-) 、 caesium carbonate 、 盐酸 作用下， 以 甲苯 、 四氢呋喃 、 水 为溶剂， 反应 102.0h， 以90%的产率得到(2R,3S,3aR)-tert-butyl 3-(4-methoxyphenyl)-2,3,3a,4-tetrahydrochromeno[4,3-b]pyrrole-2-carboxylate
  参考文献：
  名称：

  Asymmetric Phase-Transfer-Catalyzed Conjugate Addition of Glycine Imine to Exocyclic α,β-Unsaturated Ketones: Construction of Polycyclic Imines Containing Three Stereocenters

  摘要：

  We developed a facile, one-pot, multistep transformation between glycine imine and exocyclic alpha,beta-unsaturated ketones in reactions catalyzed by chiral phase-transfer catalysts (PTC). A series of polycyclic imines containing three adjacent stereocenters were obtained in good to high yields with high diastereo- and enantioselectivities. Further transformation of the imines could afford N-fused polycyclic compounds with four adjacent stereocenters.

  DOI：

  10.1021/jo300500r

文献信息

• Asymmetric Phase-Transfer-Catalyzed Conjugate Addition of Glycine Imine to Exocyclic α,β-Unsaturated Ketones: Construction of Polycyclic Imines Containing Three Stereocenters
  作者：Jing Nie、Ming-Qing Hua、Heng-Ying Xiong、Yan Zheng、Jun-An Ma

  DOI：10.1021/jo300500r

  日期：2012.5.4

  We developed a facile, one-pot, multistep transformation between glycine imine and exocyclic alpha,beta-unsaturated ketones in reactions catalyzed by chiral phase-transfer catalysts (PTC). A series of polycyclic imines containing three adjacent stereocenters were obtained in good to high yields with high diastereo- and enantioselectivities. Further transformation of the imines could afford N-fused polycyclic compounds with four adjacent stereocenters.