Abstract
A series of potential unimetal superbases BuLi–ROLi has been studied in order to increase the basicity/nucleophilicity ratio ([B/N]R) of BuLi. The best [B/N]R ratio is found with BuLi–LiDMAE. This complex base apparently metallates 2-methoxypyridine at the unexpected C-6 position. It is shown that no actual metallated species are formed in the reaction medium, the reaction occurring as the result of a common radical precursor stabilized by an aggregate cluster. Finally, as an application, C-6 substituted 2-methoxypyridines have been obtained in good to excellent yields.

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