(S)-3-[2-(3-Allyloxy-5-benzyloxy-4-methyl-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one | 141362-52-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (S)-3-[2-(3-Allyloxy-5-benzyloxy-4-methyl-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one
• CAS: 141362-52-9
• 化学式: C₂₉H₂₉NO₅
• 分子量: 471.553
• InChiKey: NEVBBAAZUKRHHL-VWLOTQADSA-N

物化性质

• 沸点：
  659.0±55.0 °C(Predicted)
• 密度：
  1?+-.0.06 g/cm3(Predicted)

反应信息

• 作为反应物：
  描述：

  (S)-3-[2-(3-Allyloxy-5-benzyloxy-4-methyl-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one 生成 (S)-3-[(R)-2-(3-Allyloxy-5-benzyloxy-4-methyl-phenyl)-2-azido-acetyl]-4-benzyl-oxazolidin-2-one 、 (S)-3-[(S)-2-(3-Allyloxy-5-benzyloxy-4-methyl-phenyl)-2-azido-acetyl]-4-benzyl-oxazolidin-2-one
  参考文献：
  名称：

  A general approach to the asymmetric synthesis of vancomycin-related arylglycines by enolate azidation

  摘要：

  The asymmetric synthesis of vancomycin-related alpha-azido arylglycines by direct azide transfer methodology is reported. Procedures for the conversion of the azides to N-protected arylglycines are provided.

  DOI：

  10.1016/s0040-4039(00)91892-6