M. Schumann et al., R-5-(ALPHA-HALOGENOBENZYL)-3,T-4-DIARYL-C -4-HYDROXY-OXAZOLIDIN-2-ONES AS RING TAUTOMERS OF YLAMINOCARBONYLOXY)-BETA-HALOGENO-DIHYDROCHALCONES, Journal fur praktische Chemie, Chemiker-Zeitung, 336(6), 1994, pp. 509-513
The reaction of chalcone halogenohydrins (1-3) with arylisocyanates do
es not stop at the stage of the rylaminocarbonyloxy-beta-halogeno-dihy
drochalcones (7), but the cyclic urethanes 4-6 are formed. Compound 7h
was synthesized independently. The structure and stereochemistry of 4
-6 and 7h were determined by C-13 n.m.r. spectroscopy.