(E)-2-(2-nitrodec-1-en-3-ynyl)thiophene

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 杂芳族化合物
• 英文名称: (E)-2-(2-nitrodec-1-en-3-ynyl)thiophene
• 英文别名: 2-[(E)-2-nitrodec-1-en-3-ynyl]thiophene
• 化学式: C₁₄H₁₇NO₂S
• 分子量: 263.36
• InChiKey: BOJFDFPTEXZIAV-OUKQBFOZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  18
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  74.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  (Z)-2-(2-bromo-2-nitrovinyl)thiophene 、 1-辛炔 在 四(三苯基膦)钯 N-甲基吗啉 、 copper(l) iodide 作用下， 以 甲苯 为溶剂， 反应 2.0h， 以86%的产率得到(E)-2-(2-nitrodec-1-en-3-ynyl)thiophene
  参考文献：
  名称：

  Stereospecific approach to α,β-disubstituted nitroalkenes via coupling of α-bromonitroalkenes with boronic acids and terminal acetylenes

  摘要：

  (Z)-alpha-Bromo-beta-substituted nitroethylenes undergo facile Suzuki coupling with aryl, heteroaryl, and vinylboronic acids in the presence of Pd(PPh3)(4) as catalyst to afford (E)-alpha,beta-disubstituted nitroethylenes in high yield (up to 95%) and complete specificity. Similar coupling of alpha-bromonitroethylenes with terminal acetylenes (Sonogashira coupling) provides a novel route to (E)-nitroenynes. These Pd-catalyzed coupling methods offer a convenient and stereospecific entry into a diverse array of synthetically and biologically useful alpha,beta-disubstituted nitroethylenes. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2007.09.012

文献信息

• Stereospecific approach to α,β-disubstituted nitroalkenes via coupling of α-bromonitroalkenes with boronic acids and terminal acetylenes
  作者：Madhu Ganesh、Irishi N.N. Namboothiri

  DOI：10.1016/j.tet.2007.09.012

  日期：2007.11

  (Z)-alpha-Bromo-beta-substituted nitroethylenes undergo facile Suzuki coupling with aryl, heteroaryl, and vinylboronic acids in the presence of Pd(PPh3)(4) as catalyst to afford (E)-alpha,beta-disubstituted nitroethylenes in high yield (up to 95%) and complete specificity. Similar coupling of alpha-bromonitroethylenes with terminal acetylenes (Sonogashira coupling) provides a novel route to (E)-nitroenynes. These Pd-catalyzed coupling methods offer a convenient and stereospecific entry into a diverse array of synthetically and biologically useful alpha,beta-disubstituted nitroethylenes. (c) 2007 Elsevier Ltd. All rights reserved.