有机化学 ›› 2014, Vol. 34 ›› Issue (3): 605-609.DOI: 10.6023/cjoc201310006 上一篇    下一篇

学术动态

烯基溴化合物的合成方法研究进展

张文生a, 许文静a, 匡春香b   

  1. a 焦作师范高等专科学校理工学院 焦作 454001;
    b 同济大学化学系 上海 200092
  • 收稿日期:2013-10-09 修回日期:2013-11-06 发布日期:2013-11-20
  • 通讯作者: 张文生,匡春香 E-mail:tongjizws@163.com
  • 基金资助:

    国家自然科学基金(No. 21272174);河南省科技厅基础和前沿研究计划(Nos. 132300410206,132300410167);焦作市科技局科技计划(No. 2012017)资助项目.

Research Advances in the Synthetic Methods of Vinyl Bromides

Zhang Wenshenga, Xu Wenjinga, Kuang Chunxiangb   

  1. a School of Technology, Jiaozuo Teachers College, Jiaozuo 454001;
    b Department of Chemistry, Tongji University, Shanghai 200092
  • Received:2013-10-09 Revised:2013-11-06 Published:2013-11-20
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 21272174), the Foundation of He'nan Scientific and Technological Committee (Nos. 132300410206, 132300410167) and the Foundation of Jiaozuo Scientific and Technological Bureau (No. 2012017).

以烯基溴化合物为代表的烯基卤代烃(1-卤代-1-烯烃)是过渡金属催化下通过C—C偶联反应构建多取代烯烃的重要合成砌块. 因此,开发简便、有效的合成烯基溴化合物的新方法越来越受到人们的重视和关注. 对按照所使用的合成原料进行分类,对近年来所报道的烯基溴化合物的合成方法进行了回顾. 所综述的主要的合成方法中所涉及的合成原料涵盖了酮类、炔类、炔丙醇类、烯基三氟甲磺酸酯类、3-芳基-2,3-二溴丙酸、苄基溴类、丙烯酸类、环丙烯类和烯丙醇类衍生物等共9类化合物.

关键词: 烯基溴化合物, 合成, 立体选择性, 区域选择性

Vinyl halides (1-halo-1-alkenes), especially vinyl bromides, represent a kind of organic synthetic blocks, which play important roles in the construction of polysubstituted alkenes through transition metal-catalyzed C—C cross-coupling reactions. Consequently, there have been much attentions in facile, efficient methods of preparing vinyl bromides. According to the types of the synthetic substrates used in the literatures, newly reported means on the synthesis of vinyl bromides in recent years are surveyed. The synthetic substrates involved in these new approaches include ketones, alkynes, propargylic alcohols, vinyl triflates, 3-aryl-2,3-dibromopropionic acids, benzyl bromides, acrylic acids, cyclopropenes and allylic alcohol derivatives, etc.

Key words: vinyl bromide, synthesis, stereoselectivity, regioselectivity