Intramolecular oxidative deselenization of acylselenoureas: a facile synthesis of benzoxazole amides and carbonic anhydrase inhibitors

A mild, efficient and one pot procedure to access benzoxazoles using easily accessible acylselenoureas as starting materials has been discovered. Mechanistic studies revealed a pH dependent intramolecular oxidative deselenization, with ring closure due to an intramolecular nucleophilic attack of a p...

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Veröffentlicht in:Organic & biomolecular chemistry 2016-01, Vol.14 (48), p.11353-11356
Hauptverfasser: Angeli, A, Peat, T S, Bartolucci, G, Nocentini, A, Supuran, C T, Carta, F
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Sprache:eng
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Zusammenfassung:A mild, efficient and one pot procedure to access benzoxazoles using easily accessible acylselenoureas as starting materials has been discovered. Mechanistic studies revealed a pH dependent intramolecular oxidative deselenization, with ring closure due to an intramolecular nucleophilic attack of a phenoxide ion. All the benzoxazoles herein reported possessed a primary sulfonamide zinc binding group and showed effective inhibitory action on the enzymes, carbonic anhydrases.
ISSN:1477-0520
1477-0539
DOI:10.1039/c6ob02299e