首页> 外文期刊>Chemistry Select >’’One-Pot’’ Selective Synthesis of 3,4-Disubstituted Pyrroles and Benzo[f]indole-4,9-diones from 1,3-Indanedione, Aromatic Aldehydes and TosMIC
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’’One-Pot’’ Selective Synthesis of 3,4-Disubstituted Pyrroles and Benzo[f]indole-4,9-diones from 1,3-Indanedione, Aromatic Aldehydes and TosMIC

机译:从1,3- indanedione,芳族醛和tosmicic中,'一锅’选择性合成3,4-二级吡咯和苯并[f] indole-4,9-二酮

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摘要

A variety of 3,4-disubstituted pyrroles and benzo[f]indole-4,9- diones have been selectively synthesized from readily available aromatic aldehydes, 1,3-Indanedione and tosylmethyl isocyanide (TosMIC) by a one-pot procedure in high yields. This methodology features operationally simple, practical with broad substrate scope and usage of easy to handle reagents. The one-pot sequential reactions proposed to proceeds through a tandem in situ generated chalcones and [3+2]- cycloaddition/ring cleavage or expansion process.
机译:已经通过一台醛,1,3-二酮和苯并[F]吲哚-4,9-二酮从易于使用的芳族醛,1,3- indanedione和tosylmethylmethylsocyanide(Tosmic)中选择性合成。 产量。 该方法具有操作简单,实用的,具有广泛的底物范围和易于处理试剂的使用。 提出的一盘顺序反应是通过串联的原位生成的chalcone和[3+2] - 环加成/环裂解或膨胀过程进行的。

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