(R)-tert-butyl 3-acetoxy-14-methylpentadecanoate | 936703-34-3

• 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: (R)-tert-butyl 3-acetoxy-14-methylpentadecanoate
• 英文别名: tert-butyl (3R)-3-acetyloxy-14-methylpentadecanoate
• CAS: 936703-34-3
• 化学式: C₂₂H₄₂O₄
• 分子量: 370.573
• InChiKey: WAEVWLNNFFEBRQ-HXUWFJFHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.4
• 重原子数：
  26
• 可旋转键数：
  17
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (R)-tert-butyl 3-acetoxy-14-methylpentadecanoate 在 三氟乙酸 、 potassium carbonate 作用下， 以 二氯甲烷 、 甲醇 为溶剂， 反应 12.0h， 以90%的产率得到(R)-3-hydroxy-14-methylpentadecanoic acid
  参考文献：
  名称：

  Total Synthesis of Plusbacin A₃:  A Depsipeptide Antibiotic Active Against Vancomycin-Resistant Bacteria

  摘要：

  Plusbacin A(3) is a depsipeptide antibiotic isolated from Pseudomonas sp. Although the stereochemistry at the lactone stereocenter had not been determined, biological evaluation of this compound demonstrated it to have promising antibacterial activity against vancomycin-resistant enterococci. Its mechanism of action remains to be conclusively established, but it is believed to exert its antibiotic effect through inhibition of bacterial cell wall biosynthesis. In this paper, we describe the first total synthesis of plusbacin A(3) and assign the stereochemistry for the remaining unassigned lactone stereocenter.

  DOI：

  10.1021/ja068455x
• 作为产物：
  描述：

  (S)-tert-butyl 3-acetoxy-14-methylpentadec-4-enoate 在 palladium on activated charcoal 氢气 作用下， 以 乙醇 为溶剂， 反应 24.0h， 以98%的产率得到(R)-tert-butyl 3-acetoxy-14-methylpentadecanoate
  参考文献：
  名称：

  Total Synthesis of Plusbacin A₃:  A Depsipeptide Antibiotic Active Against Vancomycin-Resistant Bacteria

  摘要：

  Plusbacin A(3) is a depsipeptide antibiotic isolated from Pseudomonas sp. Although the stereochemistry at the lactone stereocenter had not been determined, biological evaluation of this compound demonstrated it to have promising antibacterial activity against vancomycin-resistant enterococci. Its mechanism of action remains to be conclusively established, but it is believed to exert its antibiotic effect through inhibition of bacterial cell wall biosynthesis. In this paper, we describe the first total synthesis of plusbacin A(3) and assign the stereochemistry for the remaining unassigned lactone stereocenter.

  DOI：

  10.1021/ja068455x