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首页> 外文期刊>Organic letters >Palladium-Catalyzed Site-Selective Benzocylization of Aromatic Acids with o-Fluoro-Substituted Diaryliodonium Salts toward 3,4-Benzocoumarins
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Palladium-Catalyzed Site-Selective Benzocylization of Aromatic Acids with o-Fluoro-Substituted Diaryliodonium Salts toward 3,4-Benzocoumarins

机译:钯催化的位点 - 选择性苯并碘化芳族酸与O-氟取代的二芳碘鎓盐朝向3,4-苯并辛酸

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摘要

By using 2-fluoro-substituted diaryliodonium salts, a novel benzocylization has been accomplished for the synthesis of 3,4-benzocoumarin derivatives via a cascade of ortho-arylation and defluorination in the presence of palladium catalysts. The reaction exhibits a broad compatibility of readily available aromatic acids with an excellent level of site-selectivity. Mechanistic investigations revealed a unique reactivity of carboxylic acid directed arylation by followed nucleophilic substitution of aromatic fluoride in the present system.
机译:通过使用2-氟取代的二芳碘鎓盐,已经通过在钯催化剂存在下通过级联和偏氟化级联合成3,4-苯罗米林衍生物来完成新的苯并噻吩。 该反应表现出具有优异的位点选择性水平的易含芳族酸的广泛相容性。 机械研究揭示了本系统中芳族氟化物的亲核取代羧酸指导芳族的独特反应性。

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  • 来源
    《Organic letters》 |2020年第12期|共5页
  • 作者单位

    East China Univ Sci &

    Technol Key Lab Adv Mat Inst Fine Chem Sch Chem &

    Mol Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol Key Lab Adv Mat Inst Fine Chem Sch Chem &

    Mol Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol Key Lab Adv Mat Inst Fine Chem Sch Chem &

    Mol Engn Shanghai 200237 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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