Catalyst-Free Regioselective C‑3 Thiocyanation of Imidazopyridines
收藏NIAID Data Ecosystem2026-03-09 收录
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A direct and straightforward approach for highly regioselective thiocyanation of imidazoheterocycles through sp2 C–H functionalization has been realized at room temperature. Various C-3 thiocyanated imidazopyridines are formed in moderate to good yield. The present method exhibits a mild and selective access to a variety of imidazopyridine derivatives of pharmacological interest.
创建时间：
2016-02-12
