Author:
Li Zhong,Yang Hongchen,Chen Yuce,Xu Xiaoyong
Abstract
AbstractA convenient and efficient protocol has been developed for the synthesis of thiocyanated aminonitroalkenes and 2,4,5-trisubstituted thiazoles/selenazoles from β-aminonitroalkenes and N‑thio/selenocyanatosaccharin. This method features simple operation, mild reaction conditions, short reaction time, good functional group compatibility, and metal-free characteristics. The broad applications of polysubstituted thiazoles/selenazoles in organic and medicinal chemistry make this protocol much more practical.
Funder
Shanghai Municipal Education Commission
Fundamental Research Funds for Central Universities
National Key Research Program of China
Cited by
1 articles.
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