N-碘代丁二酰亚胺(NIS)参与的碘化反应最新研究进展
Recent Progress in N-Iodosuccinimide(NIS)-Mediated Iodination Reactions
曹同阳 1李玮 2王力竞2
作者信息
- 1. 河北大学化学与材料科学学院 河北保定 071002
- 2. 河北大学化学与材料科学学院 河北保定 071002;药物化学与分子诊断教育部重点实验室 河北省化学生物学重点实验室 河北保定 071002
- 折叠
摘要
有机碘化合物是一类非常重要的功能性分子,其合成研究具有重要意义.鉴于N-碘代丁二酰亚胺(NIS)具有反应活性高、廉价易得和环境友好等优点,一直以来都是碘化反应的优选碘试剂.近年来利用NIS参与的碘化反应制备有机碘化合物有了重要新进展,引起了极大地关注.综述了这一领域的最新研究进展,主要包括NIS与芳烃/末端炔烃的C—H碘化反应、NIS与不饱和化合物和亲核试剂的碘化双官能团化反应,以及NIS与不饱和化合物的串联碘环化反应.
Abstract
Organoiodine compounds belong to a very important class of functional molecules and their synthesis research is of great significance.Given the advantages of N-iodosuccinimide(NIS)with high reactivity,cheap and easy to get and environmental friendliness,it has always been the preferred iodine reagent for iodization,and in recent years,the preparation of organic iodine compounds by iodization reaction with NIS has made great progress,which has received considerable interest.To this end,the research progress is summarized,including the C—H iodization of NIS and aromatics/terminal alkynes,iodine difunctionalization between NIS and unsaturated compounds with nucleophiles,and cascade iodocyclization between NIS and unsaturated compounds.
关键词
碘化反应/N-碘代丁二酰亚胺(NIS)/有机碘化合物Key words
iodization/N-iodosuccinimide/organoiodine compounds引用本文复制引用
基金项目
国家自然科学基金(21702043)
河北省自然科学基金(B2021201035)
出版年
2024
NETL
NSTL
万方数据