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S-Methyl p-toluenethiosulfonate

KETOALDEHYDES S-Methyl p-toluenethiosulfonate. l-Methylthio-3-methyoxypro-pane. [Pg.732]

A variety of (dithioperoxo)thioic acid esters 220 were synthesized in moderate to good yields by reacting dithioate magnesium halides 221 with S-alkyl p-toluenethiosulfonates 222 or S-methyl methanethiosulfonates (223) (Scheme 43) [136,137]. Oxidation of 220 with m-CPBA gave the sulfines 224 as an E-Zgeometrical mixture [136]. These sulfines isomerized to acyl trisulfides (R C(O)-S3R ) after 10 days at room temperature. [Pg.219]

See other pages where S-Methyl p-toluenethiosulfonate is mentioned: [Pg.400]    [Pg.401]    [Pg.402]    [Pg.789]    [Pg.203]    [Pg.204]    [Pg.588]    [Pg.400]    [Pg.401]    [Pg.402]    [Pg.789]    [Pg.203]    [Pg.204]    [Pg.588]   
See also in sourсe #XX -- [ Pg.400 , Pg.401 , Pg.402 ]

See also in sourсe #XX -- [ Pg.400 , Pg.401 , Pg.402 ]



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S-Methylation

Toluenethiosulfonate

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