Affiliation:
1. Department of Chemistry Federal University of Santa Maria (UFSM) 97105 900 Santa Maria RS Brazil
2. Laboratory of Biotechnology of Natural and Synthetic Products University of Caxias do Sul (UCS) 95070 560 Caxias do Sul RS Brazil
Abstract
AbstractA mild and regioselective approach to the direct selenylation of 4‐(N‐substituted‐amino)‐2H‐chromen‐2‐ones employing Selectfluor® and diorganyl diselenides has been developed. The reactions were carried out under metal‐free conditions, without the need for special devices, and using NaHCO3 as a mild base at room temperature under air. This approach has been suitable for a wide substrate scope affording the 3‐selenyl‐4‐(N‐substituted‐amino)‐2H‐chromen‐2‐ones in good to excellent yields.
Cited by
1 articles.
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