(+/-)-4,4-dimethyl-2-(1-tritylaziridin-2-yl)-4,5-dihydrooxazole | 949563-18-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: (+/-)-4,4-dimethyl-2-(1-tritylaziridin-2-yl)-4,5-dihydrooxazole
• 英文别名: 4,4-dimethyl-2-(1-tritylaziridin-2-yl)-5H-1,3-oxazole
• CAS: 949563-18-2
• 化学式: C₂₆H₂₆N₂O
• 分子量: 382.505
• InChiKey: ZCPPIWUINWGAKX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.87
• 重原子数：
  29.0
• 可旋转键数：
  5.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  24.6
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  (+/-)-4,4-dimethyl-2-(1-tritylaziridin-2-yl)-4,5-dihydrooxazole 在 四甲基乙二胺 、 仲丁基锂 、 三氟乙酸 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 环己烷 、 水 为溶剂， 反应 50.0h， 生成 (1RS,4SR,5SR)-4-(4-bromophenyl)-6-trityl-3-oxa-6-aza-bicyclo[3.1.0]hexan-2-one
  参考文献：
  名称：

  Regio- and Stereoselective Lithiation of Terminal Oxazolinylaziridines:  The Aziridine N-Substituent and the Oxazolinyl Group Effect

  摘要：

  The regioselective lithiation of terminal oxazolinylaziridines has been investigated. The steric hindrance of the nitrogen substituent in 1-trityl-2-oxazolinylaziridine 3a, combined with the coordinating ability of the oxazolinyl group, causes beta-lithiation, whereas a completely regioselective alpha-lithiation is observed with the much less sterically demanding 1-benzyl-2-oxazolinylaziridine 3c and a competition between alpha- and beta-lithiation occurs with 1-cumyl-2-oxazolinylaziridine 3b in which the N-substituent has a steric hindrance in between the trityl and the benzyl groups. The application of the lithiation-trapping sequence for the preparation of enantioenriched 2,3-cis-disubstituted oxazolinylaziridines and aziridino-gamma-lactones is also reported.

  DOI：

  10.1021/ol071264u
• 作为产物：
  描述：

  三苯基甲基溴 在 lanthanum(III) chloride 、 正丁基锂 、 二乙胺基三氟化硫 、 sodium hydride 作用下， 以 四氢呋喃 、 二氯甲烷 、 环己烷 、 甲苯 为溶剂， 反应 39.0h， 生成 (+/-)-4,4-dimethyl-2-(1-tritylaziridin-2-yl)-4,5-dihydrooxazole
  参考文献：
  名称：

  Regio- and Stereoselective Lithiation of Terminal Oxazolinylaziridines:  The Aziridine N-Substituent and the Oxazolinyl Group Effect

  摘要：

  The regioselective lithiation of terminal oxazolinylaziridines has been investigated. The steric hindrance of the nitrogen substituent in 1-trityl-2-oxazolinylaziridine 3a, combined with the coordinating ability of the oxazolinyl group, causes beta-lithiation, whereas a completely regioselective alpha-lithiation is observed with the much less sterically demanding 1-benzyl-2-oxazolinylaziridine 3c and a competition between alpha- and beta-lithiation occurs with 1-cumyl-2-oxazolinylaziridine 3b in which the N-substituent has a steric hindrance in between the trityl and the benzyl groups. The application of the lithiation-trapping sequence for the preparation of enantioenriched 2,3-cis-disubstituted oxazolinylaziridines and aziridino-gamma-lactones is also reported.

  DOI：

  10.1021/ol071264u