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PIII /PV =O Catalyzed Cascade Synthesis of N-Functionalized Azaheterocycles.

Trevor V NykazaGen LiJunyu YangMichael R LuzungAlexander T Radosevich
Published in: Angewandte Chemie (International ed. in English) (2020)
An organocatalytic method for the modular synthesis of diverse N-aryl and N-alkyl azaheterocycles (indoles, oxindoles, benzimidazoles, and quinoxalinediones) is reported. The method employs a small-ring organophosphorus-based catalyst (1,2,2,3,4,4-hexamethylphosphetane P-oxide) and a hydrosilane reductant to drive the conversion of ortho-functionalized nitroarenes into azaheterocycles through sequential intermolecular reductive C-N cross coupling with boronic acids, followed by intramolecular cyclization. This method enables the rapid construction of azaheterocycles from readily available building blocks, including a regiospecific approach to N-substituted benzimidazoles and quinoxalinediones.
Keyphrases
  • room temperature
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  • energy transfer
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  • high resolution
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