期刊
ACS OMEGA
卷 3, 期 12, 页码 17540-17546出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsomega.8b02740
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资金
- Indian National Science Academy, New Delhi
Bicyclic arenyl selenides are of much importance because of their pharmaceutical applications. A simple method for their synthesis has been developed by a reaction of 2-naphthol and styrenyl selenocyanate/diaryl diselenide in the presence of a base at room temperature. The selenation occurs exclusively at the 1-position of 2-naphthol unit. The reactions are relatively fast (2-4 h) and high yielding. A library of substituted naphthyl styrenyl and naphthyl aryl selenides are obtained by this procedure.
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