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Thioethers from carbocations

Chemoselective oxidation of 3-arylsul-fenylmethyl-A -cephem affords 3-meth-oxymethyl-A -cephem in an anodic substitution. From the two thioethers, the arylthio group is more easily oxididized to a radical cation, that then undergoes cleavage to a thiyl radical and a carbocation (Fig. 31) [152]. [Pg.418]


See other pages where Thioethers from carbocations is mentioned: [Pg.107]    [Pg.115]    [Pg.135]    [Pg.1234]    [Pg.325]    [Pg.185]    [Pg.125]   
See also in sourсe #XX -- [ Pg.107 ]

See also in sourсe #XX -- [ Pg.107 ]




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