6'-azidohexyl 2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside | 1096120-02-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 6'-azidohexyl 2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
• 英文别名: (2R,4aR,6S,7S,8S,8aS)-6-(6-azidohexoxy)-2-phenyl-7-phenylmethoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-8-ol
• CAS: 1096120-02-3
• 化学式: C₂₆H₃₃N₃O₆
• 分子量: 483.565
• InChiKey: SFYNDTVOXVILIZ-RMPBONJYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  35
• 可旋转键数：
  12
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  80.7
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  6'-azidohexyl 2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 、 phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside 在 N-碘代丁二酰亚胺 、 三氟甲磺酸三甲基硅酯 作用下， 以 二氯甲烷 为溶剂， 反应 0.17h， 以80%的产率得到6'-azidohexyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
  参考文献：
  名称：

  Sonication-Assisted Oligomannoside Synthesis

  摘要：

  We have investigated the use of sonication for the synthesis of oligomannosides. A convenient sonication-mediated glycosylation protocol that is applicable to traditional glycosylation methods has been developed. This protocol can be applicable for activating glycosyl donors that are known to have low reactivity which enable the synthesis of oligomannosides of particular biological interest with the same efficiency.

  DOI：

  10.1021/jo8019835
• 作为产物：
  描述：

  6'-azidohexyl 4,6-O-benzylidene-α-D-mannopyranoside 、 溴甲苯 在 sodium hydroxide 、 四丁基硫酸氢铵 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 15.0h， 以58%的产率得到6'-azidohexyl 2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
  参考文献：
  名称：

  Sonication-Assisted Oligomannoside Synthesis

  摘要：

  We have investigated the use of sonication for the synthesis of oligomannosides. A convenient sonication-mediated glycosylation protocol that is applicable to traditional glycosylation methods has been developed. This protocol can be applicable for activating glycosyl donors that are known to have low reactivity which enable the synthesis of oligomannosides of particular biological interest with the same efficiency.

  DOI：

  10.1021/jo8019835