methyl (2S)-2-[[(2R)-2-[(2R,3S,4R,5R,6R)-5-acetamido-3-acetyloxy-2-(acetyloxymethyl)-6-phosphonooxyoxan-4-yl]oxypropanoyl]amino]propanoate | 1093956-94-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl (2S)-2-[[(2R)-2-[(2R,3S,4R,5R,6R)-5-acetamido-3-acetyloxy-2-(acetyloxymethyl)-6-phosphonooxyoxan-4-yl]oxypropanoyl]amino]propanoate
• CAS: 1093956-94-5
• 化学式: C₁₉H₃₁N₂O₁₄P
• 分子量: 542.434
• InChiKey: GQGKGOKDWAAWOE-QUGMGVNNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -2.5
• 重原子数：
  36
• 可旋转键数：
  14
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  222
• 氢给体数：
  4
• 氢受体数：
  14

反应信息

• 作为反应物：
  描述：

  methyl (2S)-2-[[(2R)-2-[(2R,3S,4R,5R,6R)-5-acetamido-3-acetyloxy-2-(acetyloxymethyl)-6-phosphonooxyoxan-4-yl]oxypropanoyl]amino]propanoate 在 lithium hydroxide 作用下， 以 水 为溶剂， 反应 24.0h， 生成
  参考文献：
  名称：

  Total synthesis of uridine diphosphate-N-acetylmuramoyl-l-alanine

  摘要：

  The first total synthesis of uridine diphosphate N-acetylmuramoyl-L-alanine in 13% overall yield is presented. The 11-step synthetic route is based on the synthetic strategy used for the synthesis Of Uridine diphosphate N-acetylmuramic acid, the MurC ligase Substrate. However, all unexpected amide bond cleavage under basic conditions demanded crucial modifications of the final synthetic steps. The total chemical synthesis Of MurD ligase substrate provides an excellent alternative to chemoenzymatic synthesis. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2008.09.029
• 作为产物：
  描述：

  methyl (S)-2-(2-(R)-(2-acetamido-2-deoxy-4,6-di-O-acetyl-1-O-diphenoxyphosphoryl-3-α-D-glucopyranosyloxy)propanamido)propanoate 在 platinum(IV) oxide 、 氢气 作用下， 反应 24.5h， 生成 methyl (2S)-2-[[(2R)-2-[(2R,3S,4R,5R,6R)-5-acetamido-3-acetyloxy-2-(acetyloxymethyl)-6-phosphonooxyoxan-4-yl]oxypropanoyl]amino]propanoate
  参考文献：
  名称：

  Total synthesis of uridine diphosphate-N-acetylmuramoyl-l-alanine

  摘要：

  The first total synthesis of uridine diphosphate N-acetylmuramoyl-L-alanine in 13% overall yield is presented. The 11-step synthetic route is based on the synthetic strategy used for the synthesis Of Uridine diphosphate N-acetylmuramic acid, the MurC ligase Substrate. However, all unexpected amide bond cleavage under basic conditions demanded crucial modifications of the final synthetic steps. The total chemical synthesis Of MurD ligase substrate provides an excellent alternative to chemoenzymatic synthesis. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2008.09.029