Reactions of eight trifluoromethyl substituted pyridines with alkyllithium reagents were examined. 3-Trifluoromethylpyridine, 3, 4-, and 3, 5-bis (trifluoromethyl) pyridines undergo regioselective lithiation at the 2-position thus providing an easy access to 2-functionalised trifluoromethylpyridines. The reactions of 2-trifluoromethylpyridine, 2, 4-, 2, 6-bis (trifluoromethyl)-pyridines and 2, 4, 6-tris (trifluoromethyl) pyridine result exclusively by ...