2-Butyl-5-<2-<<3-(ethylthio)propyl>thio>ethyl>-2-cyclopentenone | 143144-34-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-Butyl-5-<2-<<3-(ethylthio)propyl>thio>ethyl>-2-cyclopentenone
• 英文别名: 2-Butyl-5-[2-(3-ethylsulfanylpropylsulfanyl)ethyl]cyclopent-2-en-1-one
• CAS: 143144-34-7
• 化学式: C₁₆H₂₈OS₂
• 分子量: 300.53
• InChiKey: LWBXSXSTFUBCMY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  19
• 可旋转键数：
  11
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.81
• 拓扑面积：
  67.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  3-(3-Butenylthio)propan-1-ol 在 六甲基磷酰三胺 、 sodium hydride 作用下， 以 甲苯 为溶剂， 反应 2.25h， 生成 2-Butyl-5-<2-<<3-(ethylthio)propyl>thio>ethyl>-2-cyclopentenone
  参考文献：
  名称：

  Studies on the use of bidentate ligands in the directed Pauson-Khand reaction

  摘要：

  The use of bidentate ligands in the directed Pauson-Khand reaction was investigated. Substrates with a three-carbon linkage between the two heteroatoms gave better results than substrates containing two-carbon tethers. Higher yields and better regioselectivities were observed with thioamines and bisthioethers compared to diamines. Overall, only a few bidentate substrates showed marked improvements over previous results obtained with analogous monodentate compounds. Rationalizations based on the possible modes of cycloaddition operative for the various substrates studied are presented.

  DOI：

  10.1021/jo00045a021

文献信息

• Studies on the use of bidentate ligands in the directed Pauson-Khand reaction
  作者：Marie E. Krafft、Carmelinda A. Juliano

  DOI：10.1021/jo00045a021

  日期：1992.9

  The use of bidentate ligands in the directed Pauson-Khand reaction was investigated. Substrates with a three-carbon linkage between the two heteroatoms gave better results than substrates containing two-carbon tethers. Higher yields and better regioselectivities were observed with thioamines and bisthioethers compared to diamines. Overall, only a few bidentate substrates showed marked improvements over previous results obtained with analogous monodentate compounds. Rationalizations based on the possible modes of cycloaddition operative for the various substrates studied are presented.