The Methyl Group as a Source of Structural Diversity in Heterocyclic Chemistry: Side Chain Functionalization of Picolines and Related Heterocycles

The reaction of 2-picoline at the methyl group with NDA and KDA followed by dimethyldisulfide trapping
furnished, respectively, dithioacetals and trithioortho esters with high selectivity. The method was
successfully applied to other methyl-substituted pyridines, quinolines, and pyrazines. Dithioketals were
prepared by a one-pot procedure involving the reaction of metalated 2-picoline with 2 equiv of
dimethyldisulfide followed by in situ trapping with a second electrophile. All of the generated thio-substituted compounds were efficiently transformed in presence of mercury salts or under oxidizing
conditions to other functional groups comprising aldehydes, ketones, ketals, thiol esters, orthoesters, and
esters.