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The reaction of (-)1R or (+)-1S-tricarbonyl(2-substituted benzaldehyde)chro
mium complexes with tertbutylmethanesulfonamide dianion afforded, after dec
omplexation and intramolecular cyclization the enantiomerically pure N-tert
-butyl-3-(2-phenyl substituted)-1,2-thiazetidine 1,1 dioxide derivatives. T
he hydrolytic ring opening gave the corresponding enantiopure beta-aminosul
fonic acid. (C) 1999 Elsevier Science Ltd. All rights reserved.