Lewis base catalyzed, enantioselective, intramolecular sulfenoamination of olefins.

ABSTRACT: A method for the enantioselective, intramolecular sulfenoamination of various olefins has been developed using a chiral BINAM-based selenophosphoramide, Lewis base catalyst. Terminal and trans disubstituted alkenes afforded pyrrolidines, piperidines, and azepanes in high yields and high enantiomeric ratios via enantioselective formation and subsequent stereospecific capture of the thiiranium intermediate with the pendant tosyl-protected amine.

SUBMITTER: Denmark SE 

PROVIDER: S-EPMC4073881 | biostudies-literature | 2014 Jun

REPOSITORIES: biostudies-literature