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Disulfides, cyclic

Thiols and disulfides Cyclic and acyclic sulfides Mercapto-purines, -pyrimidines, -imidazoles Dithio acids and dithiocarbamides Thiocarbamides and thioamides... [Pg.182]

Partial desulfurization. Disulfides (cyclic, benzylic, aralkyl, and dialkyl) are converted into sulfides by reaction with the reagent at 25-80°.3 For example, when dibenzyl disulfide is treated with a 10% excess of the phosphine in refluxing benzene... [Pg.380]

Disulfide Cyclic Allylic Sulfide cr-Oxyacrylate Vinylsulfone... [Pg.45]

Montaudo and co-workers [12] identified the volatile products upon the thermal degradation of polystyrene disulfide using Py-MS and flash Py-MS. Using Py-MS they identified cyclic styrene disulfide, diphenyldithiene, styrene, and by flash Py-MS they identified cyclic styrene disulfide, cyclic styrene disulfide and diphenylthiophene, the latter compound not being found in direct Py-MS experiments. [Pg.164]

See other pages where Disulfides, cyclic is mentioned: [Pg.304]    [Pg.304]    [Pg.197]    [Pg.847]    [Pg.413]    [Pg.45]    [Pg.867]    [Pg.129]    [Pg.286]    [Pg.282]    [Pg.296]    [Pg.299]   
See also in sourсe #XX -- [ Pg.89 ]

See also in sourсe #XX -- [ Pg.105 ]



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Cyclic disulfides, ring-opening

Cyclic disulfides, ring-opening polymerization

Disulfide cyclic

Disulfide cyclic

Disulfides, cyclic, photolysis

Disulfides, cyclic, polydisulfides

Dithiols disulfides, cyclic

Formation of Cyclic Disulfides

Radical ring-opening cyclic disulfides

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