4-{5-[2-((R)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-oxo-ethyl]-2-benzyloxy-3-[((E)-4-propenyl)-phenoxy]-phenoxy}-benzonitrile | 141362-55-2

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物
• 英文名称: 4-{5-[2-((R)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-oxo-ethyl]-2-benzyloxy-3-[((E)-4-propenyl)-phenoxy]-phenoxy}-benzonitrile
• CAS: 141362-55-2
• 化学式: C₄₁H₃₄N₂O₆
• 分子量: 650.731
• InChiKey: BWHBVNXRBWTGIF-NTQHZXOKSA-N

反应信息

• 作为反应物：
  描述：

  4-{5-[2-((R)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-oxo-ethyl]-2-benzyloxy-3-[((E)-4-propenyl)-phenoxy]-phenoxy}-benzonitrile 生成 4-{5-[(S)-1-Azido-2-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-oxo-ethyl]-2-benzyloxy-3-[((E)-4-propenyl)-phenoxy]-phenoxy}-benzonitrile 、 4-{5-[(R)-1-Azido-2-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-oxo-ethyl]-2-benzyloxy-3-[((E)-4-propenyl)-phenoxy]-phenoxy}-benzonitrile
  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