有机化学 ›› 2026, Vol. 46 ›› Issue (6): 2327-2336.DOI: 10.6023/cjoc202511006 上一篇    下一篇

综述与进展

自由基串联反应合成1,3-苯并恶嗪研究进展

鄢东a, 何卫保a, 唐裕才d, 辛翠b,*(), 杨梓c,*(), 陈祥e,*()   

  1. a 湖南化工职业技术学院 技术与职业教育研究中心 湖南株洲 412000
    b 湖南警察学院 食药环及毒品检验技术湖南省普通高等学校重点实验室 长沙 410138
    c 长沙医学院 功能核酸基础与临床湖南省普通高校重点实验室 长沙 410219
    d 湖南文理学院化学与材料工程学院 湖南常德 415000
    e 南华大学化学化工学院 湖南衡阳 421001
  • 收稿日期:2025-11-11 修回日期:2026-01-28 发布日期:2026-02-28
  • 通讯作者: 辛翠, 杨梓, 陈祥
  • 基金资助:
    湖南省自然科学基金(2023JJ40528)

Research Progress in the Synthesis of 1,3-Benzoxazine via Radical Cascade Reaction

Dong Yana, Weibao Hea, Yucai Tangd, Cui Xinb,*(), Zi Yangc,*(), Xiang Chene,*()   

  1. a Research Center for Technical and Vocational Education Studies, Hunan Chemical Vocational Technology College, Zhuzhou, Hunan 412000
    b Key Laboratory of Food & Environment & Drug Monitoring and Testing of Universities in Hunan Province, Hunan Police Academy, Changsha 410138
    c Hunan Provincial University Key Laboratory of the Fundamental and Clinical Research on Functional Nucleic Acid, Changsha Medical University, Changsha 410219
    d College of Chemistry and Materials Engineering, Hunan University of Arts and Science, Changde, Hunan 415000
    e School of Chemistry and Chemical Engineering, University of South China, Hengyang, Hunan 421001
  • Received:2025-11-11 Revised:2026-01-28 Published:2026-02-28
  • Contact: Cui Xin, Zi Yang, Xiang Chen
  • Supported by:
    Natural Science Foundation of Hunan Province(2023JJ40528)

苯并恶嗪作为一类含氮氧杂环的重要结构单元, 广泛存在于药物分子与功能材料中, 尤其在药物研发领域, 其展现出抗炎、抗真菌等多样的生物活性, 成为极具潜力的活性分子骨架. 不饱和芳香烃衍生物(如N-酰基-2-烯基苯胺)因结构中不饱和键与杂原子位点的协同反应性, 是自由基串联反应构建苯并恶嗪骨架的优良原料, 展现出广阔的学术研究价值与工业应用前景. 围绕光介导自由基串联反应、电化学自由基串联反应、过渡金属介导自由基串联反应三个核心方向, 系统梳理了近10年来该类化合物的自由基串联反应合成研究进展; 重点关注不同合成策略的反应机理及底物适用性范围等科学问题. 最后总结了当前研究存在的挑战, 并对其合成策略的发展方向进行了展望.

关键词: 苯并恶嗪, N-酰基-2-烯基苯胺, 自由基串联反应, 烯烃双官能团化, 光氧化还原反应

As an important structural unit containing nitrogen-oxygen heterocycles, benzoxazine widely exists in drug molecules and functional materials. Especially in the field of drug research and development, it exhibits diverse biological activities such as anti-inflammatory and antifungal properties, becoming a highly potential active molecular skeleton. Unsaturated aromatic hydrocarbon derivatives (such as N-acyl-2-alkenylanilines), due to the synergistic reactivity between unsaturated their unsaturated bonds and heteroatomic sites, are excellent raw materials for constructing benzoxazine skeletons via radical cascade reactions, showing broad academic research value and industrial application prospects. Focusing on three core directions: photo-mediated radical cascade reactions, electrochemical radical cascade reactions, and transition metal-mediated radical cascade reactions, the progress in the synthesis of such compounds via radical cascade reactions over the past 10 years is systematically reviewed. Special attention is paid to such scientific issues as the reaction mechanisms and substrate scopes of different synthetic strategies. Finally, the existing challenges in current research are summarized, and the development directions of the synthetic strategies are prospected.

Key words: benzoxazines, N-acyl-2-alkenylanilines, radical cascade reactions, difunctionalization of alkenes, photoredox reactions