摘要
含氮杂环化合物具有独特的生理和药理活性,它们的高效合成引起了广大科研工作者的研究兴趣。近年来,发展了不同的合成方法制备含氮杂环化合物。其中,硒π酸催化合成含氮杂环化合物的合成方法因反应条件温和、操作简单、区域选择性和官能团兼容性好的优点受到越来越多的关注。本文综述了近些年来硒π酸催化合成含氮杂环化合物如吲哚衍生物、四氢吡咯衍生物、二氢喹嗪衍生物、噁唑衍生物、吡唑并喹唑啉酮类衍生物、异喹啉类衍生物及2-咪唑烷酮衍生物等的研究进展。
The unique physiological and pharmacological activity of aza-heterocyclic compounds has aroused the interest of researchers.In recent years,many synthetic methods for the synthesis of aza-heterocyclic compounds have been reported.Among them,selenium-π-acid catalysis has attracted extensive attention due to mild reaction conditions,simple operation,and good regioselectivity and functional group compatibility.This short review convers the progress in the synthesis of aza-heterocyclic compounds such as indoles,pyrrolidines,dihydroquinolizidines,oxazoles,pyrazolo quinazolinones,isoquinolines,and 2-imidazolidone derivatives by selenium-π-acid catalysis.
作者
许阳
廖礼豪
赵晓丹
Xu Yang;Liao Lihao;Zhao Xiaodan(Institute of Organic Chemistry&MOE Key Laboratory of Bioinorganic and Synthetic Chemistry,School of Chemistry,Sun Yat-Sen University,Guangzhou,510275)
出处
《化学通报》
CAS
CSCD
北大核心
2020年第11期970-976,共7页
Chemistry
基金
国家自然科学基金项目(21772239,91856109)资助。
关键词
含氮杂环化合物
硒π酸催化
合成方法
Aza-heterocyclic compounds
Selenium-π-acid catalysis
Synthetic methods