| 135075-70-6

• 分子结构分类: 有机化合物
• CAS: 135075-70-6
• 化学式: C₅₁H₅₁N₃O₆S
• 分子量: 834.048
• InChiKey: SIFFWYQHZQKBRB-KLCDTGHISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.69
• 重原子数：
  61.0
• 可旋转键数：
  10.0
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  96.46
• 氢给体数：
  0.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  甲醇 、 在 硫酸 作用下， 以 氯仿 为溶剂， 反应 12.0h， 以81%的产率得到dimethyl (2R,3R,4R,5S)-3-(dimethoxymethyl)-1-(4-methylphenyl)sulfonyl-5-phenylpyrrolidine-2,4-dicarboxylate
  参考文献：
  名称：

  Diastereoselective cycloaddition of N-lithiated azomethine ylides to (E)-.alpha.,.beta.-unsaturated esters bearing a C2-symmetric imidazolidine chiral controller

  摘要：

  The 1,3-dipolar cycloaddition of N-metalated azomethine ylides to chiral (E)-3-(1,3-disubstituted 4,5-diphenylimidazolidin-2-yl)propenoates proceeded highly diastereoselectively. The previously unknown absolute configuration of optically pure 1,2-dianilino-1,2-diphenylethane was determined from the absolute configuration of the cycloadducts. What diastereotopic olefin face of the alpha,beta-unsaturated ester was attacked by the ylide was found to depend dramatically upon the nature of N substituents of the chiral controller as well as upon the bulkiness of the ester moiety of the ylide.

  DOI：

  10.1021/jo00014a028
• 作为产物：
  描述：

  富马醛酸甲酯 在 正丁基锂 、 对甲苯磺酸 、 三乙胺 作用下， 以 氯仿 为溶剂， 反应 5.0h， 生成
  参考文献：
  名称：

  Diastereoselective cycloaddition of N-lithiated azomethine ylides to (E)-.alpha.,.beta.-unsaturated esters bearing a C2-symmetric imidazolidine chiral controller

  摘要：

  The 1,3-dipolar cycloaddition of N-metalated azomethine ylides to chiral (E)-3-(1,3-disubstituted 4,5-diphenylimidazolidin-2-yl)propenoates proceeded highly diastereoselectively. The previously unknown absolute configuration of optically pure 1,2-dianilino-1,2-diphenylethane was determined from the absolute configuration of the cycloadducts. What diastereotopic olefin face of the alpha,beta-unsaturated ester was attacked by the ylide was found to depend dramatically upon the nature of N substituents of the chiral controller as well as upon the bulkiness of the ester moiety of the ylide.

  DOI：

  10.1021/jo00014a028