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J Org Chem ; 88(13): 9401-9408, 2023 Jul 07.
Artículo en Inglés | MEDLINE | ID: mdl-37272415

RESUMEN

A cascade protocol for the synthesis of aminotetrazoles have been developed by treating isonitriles, N,N-dibromoarylsulfonamides, and sodium azides in the presence of K2CO3. This metal-free process proceeds via an isolable carbodiimide intermediate at room temperature, which could further react with sodium azide and subsequently cyclizes intermolecularly to provide 5-aminotetrazoles within a short reaction time. The present protocol's remarkable achievements are the wide substrate scope, good to excellent yields, and good functional group tolerance.


Asunto(s)
Azidas , Carbodiimidas , Tetrazoles
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