Attachment of an achiral, ruthenium-based Lewis acid fragment to configurat
ionally unstable biaryl thionolactones la-lc, atropo-enantioselective reduc
tive lactone cleavage of the resulting complexes with chiral hydride reagen
ts, and subsequent decomplexation leads to axially chiral thioethers 3a-3c
with enantiomeric ratios of up to 92:8.