(1E,3E,5E)-1-bromoundeca-1,3,5-triene

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 乙烯基卤化物
• 英文名称: (1E,3E,5E)-1-bromoundeca-1,3,5-triene
• 化学式: C₁₁H₁₇Br
• 分子量: 229.16
• InChiKey: VDIWLRCSQFHHQJ-OBWVEWQSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  12
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  (1E,3E,5E)-1-bromoundeca-1,3,5-triene 在 copper(II) oxide 、 potassium selenocyanate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 以92%的产率得到2-[(E)-hept-1-enyl]selenophene
  参考文献：
  名称：

  A Direct Synthesis of Selenophenes by Cu-Catalyzed One-Pot Addition of a Selenium Moiety to (E,E)-1,3-Dienyl Bromides and Subsequent Nucleophilic Cyclization

  摘要：

  An efficient protocol for the synthesis of selenophenes and selanyl selenophenes has been achieved by a simple one-pot reaction of 1,3-dienyl bromides and 1,3-dienyl-gem-dibromides respectively with KSeCN catalyzed by CuO nanoparticles. Several aryl, alkenyl, heteroaryl, and alkyl substituted selenophenes were obtained with a broad array of functional group tolerance. This is found to be a general methodology for chalcogenophenes being effective for the synthesis of thiophenes too.

  DOI：

  10.1021/ol501820e
• 作为产物：
  描述：

  反式-2,4-癸二烯醛 在 三乙胺 、 亚磷酸二乙酯 、 三苯基膦 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 生成 (1E,3E,5E)-1-bromoundeca-1,3,5-triene
  参考文献：
  名称：

  A Direct Synthesis of Selenophenes by Cu-Catalyzed One-Pot Addition of a Selenium Moiety to (E,E)-1,3-Dienyl Bromides and Subsequent Nucleophilic Cyclization

  摘要：

  An efficient protocol for the synthesis of selenophenes and selanyl selenophenes has been achieved by a simple one-pot reaction of 1,3-dienyl bromides and 1,3-dienyl-gem-dibromides respectively with KSeCN catalyzed by CuO nanoparticles. Several aryl, alkenyl, heteroaryl, and alkyl substituted selenophenes were obtained with a broad array of functional group tolerance. This is found to be a general methodology for chalcogenophenes being effective for the synthesis of thiophenes too.

  DOI：

  10.1021/ol501820e

文献信息

• 1,6-Dibromohexa-1,3,5-triene − Stereocontrolled Synthesis of Monosubstituted and Disubstituted Hexatrienes by Palladium-Catalysed Cross-Coupling Reactions
  作者：Pierre Villiers、Nicolas Vicart、Yvan Ramondenc、Gérard Plé

  DOI：10.1002/1099-0690(200102)2001:3<561::aid-ejoc561>3.0.co;2-r

  日期：2001.2

  a versatile precursor for the synthesis of conjugated 1,3,5-trienic derivatives of controlled configuration. In this paper, we describe the stereocontrolled synthesis of E,E,Z, E,E,E and Z,E,Z isomers of α-bromo-ω-substituted-1,3,5-hexatrienes and 1,6-disubstituted-1,3,5-hexatrienes. The synthesis is based on palladium-catalysed single or double cross-coupling reactions between the three isomers − 1E

  1，6-二溴己六，1，3，5-三烯是我们先前所描述的，可通过与溴亚甲基三苯基磷烷缩合而从5-溴戊二-2，4-二烯容易地获得，是合成共轭1,3受控构型的5-三烯衍生物。在本文中，我们描述了α-溴-ω-取代-1,3,5-己三烯和1,6-二取代的E，E，Z，E，E，E和Z，E，Z异构体的立体控制合成-1,3,5-己三烯。合成基于钯催化的三种异构体-1 E， 3 E， 5 Z，1 E， 3 E， 5 E和1 Z之间的单或双交叉偶联反应，中间体1,6-二溴己-1,3,5-三烯和各种有机锌试剂的3 E， 5 Z-。
• A Direct Synthesis of Selenophenes by Cu-Catalyzed One-Pot Addition of a Selenium Moiety to (<i>E,E</i>)-1,3-Dienyl Bromides and Subsequent Nucleophilic Cyclization
  作者：Pintu Maity、Debasish Kundu、Rajdip Roy、Brindaban C. Ranu

  DOI：10.1021/ol501820e

  日期：2014.8.15

  An efficient protocol for the synthesis of selenophenes and selanyl selenophenes has been achieved by a simple one-pot reaction of 1,3-dienyl bromides and 1,3-dienyl-gem-dibromides respectively with KSeCN catalyzed by CuO nanoparticles. Several aryl, alkenyl, heteroaryl, and alkyl substituted selenophenes were obtained with a broad array of functional group tolerance. This is found to be a general methodology for chalcogenophenes being effective for the synthesis of thiophenes too.