Abstract
Reaction of chlorosulfonyl isocyanate with nitroketene aminals of imidazolidines afforded acyclic intermediates which on treatment with diisopropylamine were smoothly transformed into the corresponding 1-substituted-1,2,3,7-tetrahydro-8-nitroimidazo [1,2-a] [1,2,6] thiadiazine-7 (1H) one-5, 5-dioxides.