Highly efficient metal-free reductive coupling reactions of aldehydes and ketones with a range of nucleophiles in the presence of triflic acid (1-5 mol%) as the catalyst are presented. The reactions can be performed at ambient temperature without exclusion of moisture or air. A range of symmetrical and unsymmetrical ethers were obtained by this method in high yields and short reaction times. For the first time, the influence of additional functionalization has been studied. Furthermore, the formation of thioethers from ketones (by addition of unmodified thiols) and of sulfonamides from either aldehydes or ketones has been achieved under catalytic conditions.

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S-, and N-Nucleophiles. -Highly efficient metal-free reductive coupling reactions of aldehydes and ketones with a range of nucleophiles in the presence of triflic acid as catalyst are presented. The reactions can be performed at ambient temperature without exclusion of moisture or air. The reaction conditions are compatible with the presence of a range of functional groups such as double and triple bonds, as well as of carboxylic acids, esters and amides. -(GELLERT, B. A.; KAHLCKE, N.; FEURER, M.; ROTH*, S.; Chem. Eur.