(1R,5R)-7-methyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-2-one | 1099828-18-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 恶嗪烷类
• 英文名称: (1R,5R)-7-methyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-2-one
• CAS: 1099828-18-8
• 化学式: C₇H₁₂N₂O₂
• 分子量: 156.184
• InChiKey: OLBWNPHCSPLKIS-PHDIDXHHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.9
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  41.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  二碳酸二叔丁酯 、 (1R,5R)-7-methyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-2-one 在 吡啶 、 4-二甲氨基吡啶 作用下， 反应 17.0h， 以58%的产率得到(1R,5S)-7-methyl-2-oxo-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester
  参考文献：
  名称：

  A Flexible Route to Chiral 2-endo-Substituted 9-Oxabispidines and Their Application in the Enantioselective Oxidation of Secondary Alcohols

  摘要：

  A new and flexible route to enantiomerically pure bi- and tricyclic 9-oxabispidines has been developed with use of (1R,5S)-7-methyl-2-oxo-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester as the common late-stage intermediate. The 9-oxabispidines synthesized were evaluated as the chiral ligands in the Pd(II)-catalyzed oxidative kinetic resolution of secondary alcohols giving good to excellent selectivity factors of up to 19.

  DOI：

  10.1021/jo802409x
• 作为产物：
  描述：

  (1R,5S)-3-(4-methoxybenzyl)-7-methyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-2-one 在 甲烷磺酸 作用下， 以 甲苯 为溶剂， 反应 48.0h， 以71%的产率得到(1R,5R)-7-methyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-2-one
  参考文献：
  名称：

  A Flexible Route to Chiral 2-endo-Substituted 9-Oxabispidines and Their Application in the Enantioselective Oxidation of Secondary Alcohols

  摘要：

  A new and flexible route to enantiomerically pure bi- and tricyclic 9-oxabispidines has been developed with use of (1R,5S)-7-methyl-2-oxo-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester as the common late-stage intermediate. The 9-oxabispidines synthesized were evaluated as the chiral ligands in the Pd(II)-catalyzed oxidative kinetic resolution of secondary alcohols giving good to excellent selectivity factors of up to 19.

  DOI：

  10.1021/jo802409x