S-(+)-n-butyl-2-octyl carbonate

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机碳酸及其衍生物
• 英文名称: S-(+)-n-butyl-2-octyl carbonate
• 化学式: C₁₃H₂₆O₃
• 分子量: 230.348
• InChiKey: SPPUAFBEUQAROX-LBPRGKRZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  16.0
• 可旋转键数：
  9.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  35.53
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为产物：
  描述：

  仲辛醇 、 alkaline earth salt of/the/ methylsulfuric acid 在 4 A molecular sieve 、 immobilized lipase from Candida antarctica SP 435A 作用下， 以 吡啶 、 正己烷 为溶剂， 反应 7.0h， 生成 S-(+)-n-butyl-2-octyl carbonate
  参考文献：
  名称：

  Kinetic resolution of vinyl carbonates through a lipase-mediated synthesis of their carbonate and carbamate derivatives.

  摘要：

  Lipase from Candida antarctica was used in the synthesis of different chiral carbonates and carbamates through the enzymic resolution of the starting racemic vinyl carbonates. A striking feature was the changeover of the enantioselectivity with regard to the one showed when vinyl carbonates were used in the resolution of alcohols and amines, thus the S enantiomer of the vinyl carbonate was resolved whereas the same enzyme was selective towards R ones when resolving alcohols and amines. In this way, compounds obtained beforehand as R carbonates were now achieved as S ones with better e.e.'s and shorter reaction times.

  DOI：

  10.1016/s0040-4020(01)81561-1

文献信息

• Kinetic resolution of vinyl carbonates through a lipase-mediated synthesis of their carbonate and carbamate derivatives.
  作者：Marcos Pozo、Vicente Gotor

  DOI：10.1016/s0040-4020(01)81561-1

  日期：1993.1

  Lipase from Candida antarctica was used in the synthesis of different chiral carbonates and carbamates through the enzymic resolution of the starting racemic vinyl carbonates. A striking feature was the changeover of the enantioselectivity with regard to the one showed when vinyl carbonates were used in the resolution of alcohols and amines, thus the S enantiomer of the vinyl carbonate was resolved whereas the same enzyme was selective towards R ones when resolving alcohols and amines. In this way, compounds obtained beforehand as R carbonates were now achieved as S ones with better e.e.'s and shorter reaction times.