bis[(1S)-1-[6-(hexadecanoyloxymethyl)pyridin-2-yl]ethyl] pyridine-2,6-dicarboxylate | 183160-53-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: bis[(1S)-1-[6-(hexadecanoyloxymethyl)pyridin-2-yl]ethyl] pyridine-2,6-dicarboxylate
• CAS: 183160-53-4
• 化学式: C₅₅H₈₃N₃O₈
• 分子量: 914.279
• InChiKey: RGEYECSRPRTTBK-GSVOJQHPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  17
• 重原子数：
  66
• 可旋转键数：
  42
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  144
• 氢给体数：
  0
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  (R)-1-(6-Hydroxymethyl-pyridin-2-yl)-ethanol 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 2.75h， 生成 bis[(1S)-1-[6-(hexadecanoyloxymethyl)pyridin-2-yl]ethyl] pyridine-2,6-dicarboxylate
  参考文献：
  名称：

  Ag⁺-Specific Pyridine Podands:  Effects of Ligand Geometry and Stereochemically Controlled Substitution on Cation Complexation and Transport Functions

  摘要：

  A new series of acyclic podands was designed so that three pyridine moieties cooperatively bind a guest Ag(+). Liquid-Liquid extraction, NMR binding, and computer calculation experiments reveal that podands with three pyridine donors in a proper geometry exhibit a perfect Ag(+) specificity. They selectively extracted Ag+ in the presence of equimolar Pb(2+), CU(2+), Ni(2+), Co(2+), and Zn(2+). Introduction of two chiral centers close to the pyridine binding sites surprisingly influences the Ag(+)-binding ability of the podand. Fourteen new pyridine podands were evaluated as carriers in a liquid membrane transport system. A combination of ligand geometry and stereocontrolled substitution provides excellent Ag(+)-specific transport.

  DOI：

  10.1021/jo9721148

文献信息

• Ag⁺-Specific Pyridine Podands:  Effects of Ligand Geometry and Stereochemically Controlled Substitution on Cation Complexation and Transport Functions
  作者：Hiroshi Tsukube、Satoshi Shinoda、Jun'ichi Uenishi、Takao Hiraoka、Takahiro Imakoga、Osamu Yonemitsu

  DOI：10.1021/jo9721148

  日期：1998.6.1

  A new series of acyclic podands was designed so that three pyridine moieties cooperatively bind a guest Ag(+). Liquid-Liquid extraction, NMR binding, and computer calculation experiments reveal that podands with three pyridine donors in a proper geometry exhibit a perfect Ag(+) specificity. They selectively extracted Ag+ in the presence of equimolar Pb(2+), CU(2+), Ni(2+), Co(2+), and Zn(2+). Introduction of two chiral centers close to the pyridine binding sites surprisingly influences the Ag(+)-binding ability of the podand. Fourteen new pyridine podands were evaluated as carriers in a liquid membrane transport system. A combination of ligand geometry and stereocontrolled substitution provides excellent Ag(+)-specific transport.