(2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-6-[(2S,3R,4S,5R)-4,5-diacetoxy-2-((3R,4S,5R,6R)-4,5-diacetoxy-6-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yloxy]-3-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester | 76707-57-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-6-[(2S,3R,4S,5R)-4,5-diacetoxy-2-((3R,4S,5R,6R)-4,5-diacetoxy-6-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yloxy]-3-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester
• CAS: 76707-57-8
• 化学式: C₄₁H₅₂O₁₉
• 分子量: 848.852
• InChiKey: BEEMMPVFBKAXFL-WPZCIYATSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.93
• 重原子数：
  60.0
• 可旋转键数：
  17.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  214.57
• 氢给体数：
  0.0
• 氢受体数：
  19.0

反应信息

• 作为产物：
  描述：

  (2S,3S,4S,5R)-4,5-Bis-benzyloxy-6-[(2S,3R,4S,5R)-4,5-diacetoxy-2-((3R,4S,5R,6R)-4,5-diacetoxy-6-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yloxy]-3-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester 在 吡啶 作用下， 生成 (2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-6-[(2S,3R,4S,5R)-4,5-diacetoxy-2-((3R,4S,5R,6R)-4,5-diacetoxy-6-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yloxy]-3-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester
  参考文献：
  名称：

  Synthesis of an aldotriouronic acid derivative related to (4-N-methylglucurono)xylans

  摘要：

  DOI：

  10.1016/s0008-6215(00)84609-1