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Disulfides, diphenyl desulfurization

An attempted synthesis of thiete by thermolysis (300°) of a Diels-Alder adduct with anthracene was unsuccessful, no doubt because of the thermal instability of thiete.Thiete derivative 215 was obtained by other methods, and structure 217 was suggested as an intermediate in the desulfurization of 216. The unusual dithiolactone 218b is formally derived from a cycloaddition of carbon disulfide with acetylene 218a. " A 2-substituted-3,4-diphenyl-2H-thiete is obtained by treatment of the ylide, 8-methyl-1,3-diphenyldibenzo [e, h]-8-thiazulene, with diphenylcyclo-propenethione. 2-Methoxy-3,4-diphenyl-2H-thiete is one of several products obtained on photolysis of diphenylcyclopropenethione in methanol. ... [Pg.516]


See other pages where Disulfides, diphenyl desulfurization is mentioned: [Pg.300]    [Pg.431]    [Pg.142]    [Pg.300]    [Pg.608]    [Pg.759]    [Pg.759]    [Pg.300]    [Pg.759]    [Pg.22]   


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