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Regioselective ortho lithiation of halopyridines
Authors:Gordon W. Gribble  Mark G. Saulnier
Affiliation:Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755 U.S.A.
Abstract:
Regioselective ortho lithiation of 2-, 3-, and 4-halopyridines is achieved with lithium diisopropylamide (?78°, tetrahydrofuran) to afford, upon quenching with electrophilic reagents, 2,3- and 3,4-disubstituted pyridines in good to excellent yield.
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