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首页> 外文期刊>ACS combinatorial science >Benzhydrylamines via Base-Mediated Intramolecular sp~3 C-Arylation of N-Benzyl-2-nitrobenzenesulfonamides-Advanced Intermediates for the Synthesis of Nitrogenous Heterocycles
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Benzhydrylamines via Base-Mediated Intramolecular sp~3 C-Arylation of N-Benzyl-2-nitrobenzenesulfonamides-Advanced Intermediates for the Synthesis of Nitrogenous Heterocycles

机译:通过碱介导的N〜苄基-2-硝基苯磺酰胺的分子内sp〜3 C-芳基化反应的苯甲基胺-高级中间体,用于合成氮杂环

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摘要

N-Benzyl-2-nitrobenzcnesulfonamides underwent base-mediated intramolecular arylation at the benzyl sp~3 carbon to yield benzhydrylamines. The presence of electron withdrawing groups on the aromatic ring of the benzyl group was required to facilitate the C-arylation. Unsymmetrically substituted benzhydrylamines are advanced intermediates toward nitrogenous heterocycles, as exemplified in the syntheses of indazole oxides and quinazolines.
机译:N-苄基-2-硝基苯磺酰胺在苄基sp〜3碳上进行了碱介导的分子内芳基化反应,生成苯甲基胺。需要苄基的芳环上存在吸电子基团以促进C-芳基化。如吲哚氧化物和喹唑啉的合成中所示,不对称取代的苯甲基胺是朝向含氮杂环的高级中间体。

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