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Dimethyl sulfide ditriflate

More recently, this method has been extended to preparation of a variety of disulfonium dications from both acyclic and cyclic bis-sulfides, including very labile dications not observed when other methods were used.78 Thus, simple acyclic S-S dications were prepared by an intermolecular reaction of a monosulfide, a monosulfoxide and triflic anhydride.79 In the first step, reaction of triflic anhydride with dimethylsulfoxide generates a highly electrophilic80 complex 50 (dimethyl sulfide ditriflate).81 The latter reacts with dimethyl sulfide to give labile tetramethyldisulfonium dication 51 identified by NMR spectroscopy.79 In a similar manner, bis-(tetramethylene)disulfonium dication 52 is obtained from tetrahydrothiophene and its S-oxide (Scheme 17). [Pg.425]

The less stable dimethyl sulfide ditriflate, obtained from Tf20 and DMSO, has been used to oxidize alcohols (eq 36). ... [Pg.585]


See other pages where Dimethyl sulfide ditriflate is mentioned: [Pg.605]    [Pg.248]    [Pg.54]    [Pg.54]    [Pg.601]    [Pg.225]    [Pg.782]    [Pg.500]    [Pg.275]    [Pg.605]    [Pg.248]    [Pg.54]    [Pg.54]    [Pg.601]    [Pg.225]    [Pg.782]    [Pg.500]    [Pg.275]    [Pg.376]   
See also in sourсe #XX -- [ Pg.225 ]

See also in sourсe #XX -- [ Pg.225 ]




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Dimethyl sulfide

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