Ti(IV)-catalyzed asymmetric sulfenylation of 1,3-dicarbonyl compounds

The electrophilic enantioselective sulfenylation of 1,3-dicarbonyl compounds with phenylsulfenyl chloride is effectively catalyzed by Ti(TADDOLato)] complexes. The corresponding products are obtained in moderate to high yields. The highest ee values (up to 97 %) are obtained in toluene at room temperature and with a typical catalyst loading of 5 mol %. Bulky ester groups and sterically undemanding substituents at the alpha-position were found to be crucial structural features of the starting materials in order to assure high enantioselectivity. The absolute configuration of one of the chiral products has been determined. The stereochemical course of the reaction is similar to that of analogous Ti(TADDOLato)]-catalyzed atom-transfer reactions. A common side-reaction the sulfenylated products undergo is a deacylation leading to racemic alpha-sulfenylated esters.