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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of multiply arylated heteroarenes, including bioactive derivatives, via palladium-catalyzed direct C-H arylation of heteroarenes with (pseudo)aryl halides or aryliodonium salts
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Synthesis of multiply arylated heteroarenes, including bioactive derivatives, via palladium-catalyzed direct C-H arylation of heteroarenes with (pseudo)aryl halides or aryliodonium salts

机译:常规芳基化杂种的合成,包括生物活性衍生物,通过钯 - 催化的杂种芳烃与(假)芳基卤化物或芳碘鎓盐的直接C-H芳基化

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摘要

This review with 387 references covers the literature until the end of November 2013 on the synthesis of multiply arylated heteroarenes via highly selective palladium-catalyzed direct C-H arylation reactions of heteroarene derivatives with aryl halides or pseudohalides or aryliodonium salts. Particular attention has been made to describe the synthesis of biologically active compounds and substances that are privileged structural motifs in organic materials. The practicality, versatility, and limitations of the various developed arylation protocols are discussed. 1 Introduction 2 Synthesis of Multiply Arylated Five-Membered Hetero arenes with One Heteroatom 2.1 Multiply Arylated Furan and Benzo[b]furan Derivatives 2.2 Multiply Arylated Thiophenes and Benzo[b]thiophene Derivatives 2.3 Multiply Arylated Pyrrole and Indole Derivatives 3 Synthesis of Multiply Arylated Five-Membered Hetero arenes with Two or More Heteroatoms 3.1 Multiply Arylated Pyrazole and 2H-Indazole Derivatives 3.2 Multiply Arylated Isoxazole Derivatives 3.3 Multiply Arylated Oxazole Derivatives 3.4 Multiply Arylated Thiazole and Thiazole N-Oxide Derivatives 3.5 Multiply Arylated Imidazole and Imidazole N-Oxide Derivatives 3.6 Multiply Arylated 1,2,3-Triazole and 1,2,3-Triazole N-Oxide Derivatives 3.7 Diarylated 1,2,4-Triazole and 1,3,4-Thiadiazole Derivatives 3.8 Diarylated Sydnone, 2,1,3-Benzothiadiazole, and Tetrazole Derivatives 4 Synthesis of Multiply Arylated Six-Membered Heteroarenes 4.1 Diarylated Pyridines, Pyridine N-Oxides, and Pyrazine N-Oxides 5 Synthesis of Multiply Arylated Compounds Formed by Five-Membered Heteroarenes Fused to Five-Membered Heteroarenes 5.1 Diarylated Thieno[2,3-b]thiophenes, Imidazo[1,2-b]pyrazoles, and Thiazolo[3,2-b]-1,2,4-triazoles 6 Synthesis of Multiply Arylated Compounds Formed by Six-Membered Heteroarenes Fused to Five-Membered Hetero arenes 6.1 Diarylated Indolizines, Pyrimido[5,4-b]indolizines, Pyrrolo[2,3-b]pyridines, Pyrazolo[1,5-a]pyrimidines, Imidazo[1,2-a]pyridines, Imidazo[1,5-a]pyridines, Xanthines, Imidazo[1,2-b]tetrazines, Imidazo[1,2-a]pyrazines, and Furo[3,2-b]pyridines 7 Conclusions.
机译:本综述涉及387参考文献,涵盖了2013年11月底,通过高选择性钯催化的杂种衍生物与芳基卤化物或伪碘酸盐或亚芳基碘盐的合成乘法催化的直接C-H芳基化反应来合成乘法芳苯二甲酸盐的合成。已经特别注意描述在有机材料中具有特权结构基序的生物活性化合物和物质的合成。讨论了各种开发芳基化方案的实用性,多功能性和限制。乘法芳基化五元杂环芳烃与一个杂原子2.1乘芳基化呋喃和苯并[b]呋喃衍生物2.2乘芳基化的噻吩和苯并[b]噻吩衍生物2.3乘芳基化的吡咯并吲哚衍生物的乘法芳基化五3个合成1个介绍2合成 - 与两个或更多个杂原子3.1乘以芳基吡唑和2h-吲唑衍生物3.2乘法芳基的异恶唑衍生物3.3乘法芳基氧唑和噻唑N-氧化物衍生物3.5乘以芳基咪唑和咪唑N-氧化物衍生物3.6芳基化1,2,3-三唑和1,2,3-三唑N-氧化物衍生物3.7二酯化1,2,4-三唑和1,3,4-噻二唑衍生物3.8二酯酸锡,2,1,3-苯并噻唑,和四唑衍生物4合成乘法六元杂种4.1二酯酸吡啶,吡啶N-氧化物和吡嗪N-氧化物5的组合由五元杂戊烷形成的含芳苯胺化化合物,融合到五元杂戊烷5.1二酯化噻吩[2,3-b]噻吩,咪唑[1,2-B]吡唑和噻唑[3,2-B] -1,2 ,4-三唑醚6由六元杂种物形成的六元杂种芳烃形成的乘以芳酸酯6.1二酯化吲哚,嘧啶[5,4-B]吲哚嗪,吡咯醇[2,3-b]吡啶[1 ,5-a]吡啶胺,咪唑吡啶[1,2-a]吡啶,咪唑[1,5-a]吡啶,黄嘌呤,咪唑[1,2-b]四嗪,咪唑[1,2-a]吡嗪,和呋喃[3,2-B]吡啶7结论。

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