(-)-(2R,3S)-2-methyl-3-benzylaziridine | 158703-59-4

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: (-)-(2R,3S)-2-methyl-3-benzylaziridine
• 英文别名: (2S,3R)-2-benzyl-3-methylaziridine
• CAS: 158703-59-4
• 化学式: C₁₀H₁₃N
• 分子量: 147.22
• InChiKey: VITWGSRUBCMZAY-SCZZXKLOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  21.9
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  3-溴-4-苯基-2-丁酮 在 sodium azide 、 三苯基膦 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 24.0h， 生成 (-)-(2R,3S)-2-methyl-3-benzylaziridine
  参考文献：
  名称：

  Chemoenzymatic synthesis of chiral β-azidoalcohols. Application to the preparation of chiral aziridines and aminoalcohols

  摘要：

  From the microbiological reduction of 3-azido-2-octanone, 3-azido-4-phenyl-2-butanone and 1-azido-1-phenyl-2-propanone, homochiral isomers of the corresponding beta-azidoalcohols were prepared. These ''alpha-bichiral'' synthons were used to prepare all the stereoisomers of 2-methyl-3-n-pentylaziridine and 2-methyl-3-benzylaziridine and some homochiral aminoalcohols.

  DOI：

  10.1016/0957-4166(94)80084-7

文献信息

• Chemoenzymatic synthesis of chiral β-azidoalcohols. Application to the preparation of chiral aziridines and aminoalcohols
  作者：Pascle Besse、Henri Veschambre、Robert Chênevert、Michael Dickman

  DOI：10.1016/0957-4166(94)80084-7

  日期：1994.9

  From the microbiological reduction of 3-azido-2-octanone, 3-azido-4-phenyl-2-butanone and 1-azido-1-phenyl-2-propanone, homochiral isomers of the corresponding beta-azidoalcohols were prepared. These ''alpha-bichiral'' synthons were used to prepare all the stereoisomers of 2-methyl-3-n-pentylaziridine and 2-methyl-3-benzylaziridine and some homochiral aminoalcohols.