Abstract
Abstract The sulfonamides CF 3 SO 2 N(CH 3 )Na and CF 3 SO 2 N(H)Na have been reacted with polyfluoro cyclic, acyclic and inorganic chlorine and bromine-containing species. Nucleophilic displacement of chlorine or bromine in 1,2-dichloroperfluorocyclobutene, 1,2-dichloroperfluorocyclopentene, benzyl bromide, cyanuric chloride and oxalyl chloride has been found to occur under mild conditions to give good yields of N-substituted polyfluoroalkyl and polyfluoroaryl sulfonamides. The effects of solvent and substrate structure on the conditions necessary for reaction to occur, and the yields obtained of the desired products are discussed.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
