Additions of stabilised and semi-stabilised sulfur ylides to tosyl protected imines: are they under kinetic or thermodynamic control?

Abstract

Sulfur ylides react with imines, via betaines, to give aziridines. We sought to determine whether betaine formation was reversible in reactions of benzyl-, amide- and ester-stabilised ylides by carrying out cross-over experiments. Thus, the intermediate betaines were generated independently from the corresponding sulfonium salt in the presence of a more reactive imine (p-nitrobenzaldimine). It was found that no incorporation of the more reactive imine was observed in reactions with the benzyl-stabilised ylide, whilst >80% incorporation of the p-nitrobenzaldimine was observed from the ester- and amide-stabilised ylides. These results indicate that benzyl-stabilised ylides react irreversibly with imines but ester- and amide-stabilised react reversibly. Thus, the stereocontrolling step of the process is dependent on the type of ylide employed and the results are used to account for the different diastereoselectivities observed with the different ylides.