化学学报    

综述

基于自由基串联环化策略构建氮/氧杂中环化合物研究进展

张蒙爱, 靳皓冉, 孙凯*, 祝艳平*, 王薪*   

  1. 烟台大学 药学院 山东烟台 264005
  • 投稿日期:2025-12-30
  • 作者简介:张蒙爱,女,烟台大学药学院2024级研究生,研究方向为有机氟化学、光化学合成、自由基策略构建中环. 靳皓冉,女,烟台大学药学院2024级本科生,研究方向为有机氟化学、自由基策略中环构建. 孙凯,男,2020年入职烟台大学,研究方向为有机硒化学、自由基策略构建中环. 祝艳平,男,烟台大学化学药学院副教授,研究方向为光化学合成、金属催化碳氢键官能团化.王薪,女,2023年入职烟台大学药学院,研究方向为光化学合成、有机硒氟化学.
  • 基金资助:
    国家自然科学基金项目(52303015); 山东省自然科学基金项目(ZR2023MB135; ZR2024QB086); 烟台大学研究生科研创新基金(KGIFYTU2510).

Research Progress on Construction of Medium-Sized Nitrogen/Oxygen Heterocycles Based on Radical Cascade Cyclization Strategy

Zhang Mengai, Jin Haoran, Sun Kai*, Zhu Yanping*, Wang Xin*   

  1. School of Pharmacy, Yantai University, Yantai, Shandong 264005
  • Received:2025-12-30
  • Contact: *E-mail: sunk468@nenu.edu.cn; chemzyp@ytu.edu.cn; wangx933@nenu.edu.cn
  • Supported by:
    National Natural Science Foundation of China (52303015); Shandong Provincial Natural Science Foundation (ZR2023MB135; ZR2024QB086), Yantai University Graduate Research Innovation Fund (KGIFYTU2510).

中环(七元至十二元)化合物具有独特的分子结构和生物活性,在天然产物和药物分子中广泛存在。不过由于不利的熵、焓因素以及跨环张力影响,中环化合物的构建在有机合成领域一直存在巨大挑战。近年来,通过自由基串联环化策略构建中环化合物得到了一定的发展,具有步骤简洁、绿色高效、官能团兼容性强等诸多优点。本文总结了近年来通过自由基串联环化策略合成氮/氧杂中环化合物的研究进展,重点总结了以下两个方面:(1)分别总结了七元、八元、九元至十二元环化合物的合成策略;(2)针对代表性反应的机理、底物拓展、实际应用等内容进行了重点描述。本论文旨在为自由基串联环化策略构建氮/氧杂中环化合物提供新的合成思路,有助于其在新药研发、化工、材料等领域的应用。

关键词: 自由基, 串联环化, 中环化合物, 催化, 机理研究

Medium-sized ring (7- to 12-membered) compounds possess unique molecular structures and biological activities. Widely distributed in natural products and pharmaceutically active molecules, they hold an important position in the research of organic chemistry and medicinal chemistry. In addition, in the field of materials science, medium-sized ring compounds offer numerous possibilities for the efficient synthesis of novel functional materials by virtue of their distinctive electronic distribution and spatial configuration. However, due to unfavorable entropic and enthalpic factors, as well as high transannular strain and strong conformational flexibility, the synthesis of medium-sized ring compounds is plagued by problems such as tedious procedures, low yields and poor functional group compatibility, which severely restricts the exploration, development and application of such compounds. Therefore, it is imperative to develop efficient, economical and structurally diverse synthetic strategies for medium-sized ring compounds. In recent years, the construction of medium-sized ring compounds via radical cascade cyclization has achieved considerable progress. This strategy generates highly reactive intermediates through radical pathways to trigger multiple consecutive transformations and forge multiple chemical bonds in one step, thus enabling the efficient synthesis of medium-sized ring compounds. It boasts numerous advantages including concise procedures, green and high efficiency, excellent functional group compatibility, high atom economy, and unique regio- and stereoselectivity, thereby providing a variety of strategies for the construction, development and application of medium-sized ring compounds. This paper summarizes the recent research advances in the synthesis of Nitrogen/Oxygen-containing medium-sized heterocyclic compounds via the radical cascade cyclization strategy, with a focus on the following two aspects: (1) Separately summarizing the synthetic strategies for 7-membered, 8-membered, and 9- to 12-membered ring compounds; (2) Focusing on the elaboration of the reaction mechanisms, substrate scopes and practical applications of representative reactions. This thesis aims to provide new synthetic insights for the construction of Nitrogen/Oxygen-containing medium-sized heterocyclic compounds through the radical cascade cyclization strategy and facilitate its applications in the fields of new drug research and development, chemical engineering, materials science and other related areas.

Key words: Radical, Cascade cyclization, Medium-sized ring compounds, Catalysis, Mechanism study