Catalyst-Free Regioselective C-3 Thiocyanation of Imidazopyridines
Imidazopyridine
Surface Modification
Reaction conditions
DOI:
10.1021/acs.joc.5b01637
Publication Date:
2015-10-02T17:20:41Z
AUTHORS (8)
ABSTRACT
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 selective access variety imidazopyridine derivatives pharmacological interest.
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