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酚类衍生物作为芳基自由基前体参与的高选择性反应进展

曹中艳 金胜男 王玉霞 陈依漪 孔宪强 徐元清

大学化学2025,Vol.40Issue(4):245-252,8.
大学化学2025,Vol.40Issue(4):245-252,8.DOI:10.12461/PKU.DXHX202405186

酚类衍生物作为芳基自由基前体参与的高选择性反应进展

Advances in Highly Selective Reactions Involving Phenol Derivatives as Aryl Radical Precursors

曹中艳 1金胜男 1王玉霞 1陈依漪 2孔宪强 2徐元清1

作者信息

  • 1. 河南大学化学与分子科学学院,河南 开封 475004
  • 2. 常州工学院化工与材料学院,江苏 常州 213032
  • 折叠

摘要

Abstract

Phenols,produced at an annual volume exceeding ten million tons,are widely used in various key organic transformations due to their low cost.In introductory chemistry courses,the reactions of phenols typically involve substitutions at the electron-rich aromatic ring or the hydroxyl oxygen,leaving the inert C―O bond intact in the final products.To expand the utility of phenols,researchers have developed metal-catalyzed strategies that cleave the C―O bond by introducing activating groups at the oxygen atom,enabling efficient deoxygenative coupling reactions.However,these methods often require harsh conditions and may result in metal contamination,limiting their use in pharmaceutical and other sensitive applications.To address these limitations,recent studies have demonstrated that simple phenol derivatives can selectively cleave the inert C―O bond under mild conditions,using light or electricity to generate aryl radicals.The high reactivity and selectivity of these radicals enable novel and efficient chemical transformations,offering new strategies for the application of phenols in organic synthesis.This paper reviews recent advancements in using trifluoromethanesulfonates,phosphates,and carbonates of phenols as aryl radical precursors,discussing the challenges and breakthroughs in constructing complex molecules with high precision.This review aims to broaden the knowledge of advanced students in the field.

关键词

/惰性C―O键/选择性断裂/芳基自由基/光合成/电合成

Key words

Phenols/Inert C―O bond/Selective cleavage/Aryl radicals/Photosynthesis/Electrosynthesis

分类

社会科学

引用本文复制引用

曹中艳,金胜男,王玉霞,陈依漪,孔宪强,徐元清..酚类衍生物作为芳基自由基前体参与的高选择性反应进展[J].大学化学,2025,40(4):245-252,8.

基金项目

国家自然科学基金(22201062,22372015,22202021) (22201062,22372015,22202021)

河南大学校级教改项目(HDXJJG-2022-035) (HDXJJG-2022-035)

大学化学

1000-8438

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