Abstract
Chirality of bicyclic P4S3 skeletons has been explored by reaction of α- or β-P4S3I2 with enantiomerically pure or racemic H2NCHMePh, to give diastereomers of products with one or two exocyclic amide substituents, or of cage structures containing a bridging imide group. 31P NMR spectra show diastereomeric differences in chemical shifts of all four phosphorus atoms in the product molecules. Comparison of observed with predicted numbers of diastereomers is a useful extra tool for identification of unseparated new compounds by NMR.