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Diallyl sulphone

Kinetics of the oxidation of diallyl sulphide by singlet oxygen, and its inhibition by rubrene, have been reported. Isomerization studies in which the base-catalysed prop-2-eny 1-prop-1-enyl equilibrium for allyl sulphides, sulphoxides, and sulphones were compared have been undertaken, and isolated reports on this topic have been rationalized in terms of electronic distribution in the functional groups. [Pg.38]


See other pages where Diallyl sulphone is mentioned: [Pg.1199]    [Pg.1206]    [Pg.636]    [Pg.724]    [Pg.49]    [Pg.1199]    [Pg.1206]    [Pg.636]    [Pg.724]    [Pg.49]    [Pg.21]    [Pg.96]   
See also in sourсe #XX -- [ Pg.724 ]




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