371-77-7Relevant articles and documents
A New Method for the Synthesis of Perfluorooxaziridines. Preparation of Perfluoro-cis-2,3-dialkyloxaziridines
Petrov, Viacheslav A.,DesMarteau, Darryl D.
, p. 4754 - 4755 (1993)
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PERFLUOROALKYL DERIVATIVES OF NITROGEN. PART LIII. REACTION OF PERFLUORO(2,5-DIMETHYL-4-OXA-3,5-DIAZAHEX-2-ENE) WITH FLUORO-OLEFINS
Fisher, R.,Haszeldine, R. N.,Tipping, A. E.
, p. 155 - 164 (2007/10/02)
Thermal decomposition of the title compound at 140 deg C gives mainly nitrogen, hexafluoroacetone and tetrakistrifluoromethylhydrazine while reaction with tetrafluoroethylene and chlorotrifluoroethylene affords equimolar mixtures of the 1:1 adducts (CF3)2C=NCF2CFXON(CF3)2 and (CF3)2C=NOCFXCF2N(CF3)2 (X=F and Cl) in highly yield via four-centre addition or a radical-cage process.
Reaction of Bistrifluoromethylaminosulphenyl Chloride with Hydrocarbon Olefins and the Synthesis of Bistrifluoromethylaminosulphenylarenes
Service, Colin F.,Tipping, Anthony E.
, p. 91 - 96 (2007/10/02)
Reaction of bistrifluoromethylaminosulphenyl chloride with acyclic and alicyclic hydrocarbon olefins at -78 deg C in the dark affords 1:1 adducts of type in high yield.Treatment of diaryl disulphides with the N-bromo-amine (CF3)2NBr or of benzenesulphenyl chloride with the mercurial 2Hg provide convenient routes to bistrifluoromethylaminosulphenylarenes.