A variety of phenyl alkyl sulfides were oxidized enantioselectively with NaIO_4 in chiral micellar systems formed from eight chiral surfactants,to give optical active sulfoxides.The enantiomer excesses ranged from 1.6...A variety of phenyl alkyl sulfides were oxidized enantioselectively with NaIO_4 in chiral micellar systems formed from eight chiral surfactants,to give optical active sulfoxides.The enantiomer excesses ranged from 1.6 to 15.0%.To understand the mechanistic detail of this asymmetric oxi- dation in chiral micelle,the effects of structure both in substrates and surfactants on the optical yield of the oxidation were studied and discussed.Generally,increasing the alkyl chain length both in sur- factants and in substrates enhances the optical yield,also the surfactant with hydroxy group at its appropriate position gives better enantioselectivity,suggesting the enzymic characteristics of the chiral micelle.展开更多
文摘A variety of phenyl alkyl sulfides were oxidized enantioselectively with NaIO_4 in chiral micellar systems formed from eight chiral surfactants,to give optical active sulfoxides.The enantiomer excesses ranged from 1.6 to 15.0%.To understand the mechanistic detail of this asymmetric oxi- dation in chiral micelle,the effects of structure both in substrates and surfactants on the optical yield of the oxidation were studied and discussed.Generally,increasing the alkyl chain length both in sur- factants and in substrates enhances the optical yield,also the surfactant with hydroxy group at its appropriate position gives better enantioselectivity,suggesting the enzymic characteristics of the chiral micelle.
