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Thioethers from sulfoxides

Equimolar amounts of cyclohexanol and 1-chlorobenzotriazole warmed in methylene chloride until an exothermic reaction starts cyclohexanone. Y 70%. -The above new oxidant, a positive-chlorine compound, is potentially useful because of its easy prepn., stability, reactivity under mild conditions, and easy isolation of the products. F. e. and oxidations s. C. W. Rees and R. C. Storr, Chem. Commun. 1968, 1305 Soc. (C) 1969, 1474 S-oxygenations such as sulfoxides from thioethers s. W. D. Kingsbury and C. R. Johnson, Chem. Commun. 1969, 365. [Pg.72]

Triethylenediamine bromine complex Sulfoxides from thioethers... [Pg.327]

Sulfuryl chloride silica S02CySi02 Sulfoxides from thioethers >S >SO with SOgCl /EtOH cf. 29, 98 with wet silica gel instead of ethanol s. M. Hojo and R. Masuda, Tetrah. Let. 1976, 613 ... [Pg.360]

Sodium periodate Sulfoxides from thioethers s. 31, 971 NalOt >S >SO... [Pg.360]

Microorganisms Sulfoxides from thioethers Stereospecific oxidation... [Pg.335]

Peracetic acid (s. a. H202/CHfiOOH) Partial formation of sulfoxides from thioethers Sulfones from sulfoxides s. 13, 152 CHSC002H... [Pg.62]

Hydrogen peroxide/acetic acid (s. a. Peracetic acid) Sulfones and sulfoxides from thioethers... [Pg.62]

See other pages where Thioethers from sulfoxides is mentioned: [Pg.295]    [Pg.38]    [Pg.38]    [Pg.41]    [Pg.327]    [Pg.41]    [Pg.36]    [Pg.318]    [Pg.318]    [Pg.54]    [Pg.433]    [Pg.43]    [Pg.37]    [Pg.377]    [Pg.377]    [Pg.341]    [Pg.35]    [Pg.339]    [Pg.62]    [Pg.62]    [Pg.412]    [Pg.47]    [Pg.310]    [Pg.43]    [Pg.354]   
See also in sourсe #XX -- [ Pg.1688 ]



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From sulfoxides

From thioethers

Sulfoxides thioethers

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