Asymmetric epoxidation of unfunctionalized alkenes with ammonium and phosphonium monopersulfates catalyzed by chiral Mn(III)-salen complexes

Simple cis-disubstituted and trisubstituted alkenes were enantioselectively epoxidized in mild conditions using various Mn(III)-salen complexes as cat alysts and quaternary ammonium and phosphonium monopersulfates (Bu4NHSO5, P h4PHSO5) as oxidants together with amine N-oxides as additives. The effect of the catalyst structure on the stereochemical outcome of the epoxidation reactions was studied. Generally, the 1,2-diphenylethylenediamine-derived c omplexes were found to give higher asymmetric induction compared to their 1 ,2-diaminocyclohexane-derived counterparts. Particularly high yields of epo xides (up to 98%) and good enantiomeric excesses (ee up to 93%) were obtain ed in the epoxidation of 2,2-dialkylchromenes and trisubstituted alkenes. ( C) 2000 Elsevier Science Ltd. All rights reserved.