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Telluronic Acids

Telluronic acids have not yet been prepared. They are expected to be good oxidizing agents and to have low stability. [Pg.364]

Oxidation of the ethylene acetals of 3-aryl-3-oxo-2-propyl phenyl telluriums, which were prepared from the acetals of 3-aryl-3-oxo-2-bromopropane and arenetellurolates, with 3-chloroperoxybenzoic acid in methanol at 20° produced hydroxyethyl 2-arylpropanoates2. Tellurones were postulated as intermediates that experienced a 1,2-aryl shift and the elimination of an aryltelluro moiety. [Pg.491]

The compound could not be oxidized to a tellurone using hydrogen peroxide, sodium periodate, or 3-chloroperoxybenzoic acid as oxidizing agents1. [Pg.826]

See other pages where Telluronic Acids is mentioned: [Pg.152]    [Pg.364]    [Pg.364]    [Pg.364]    [Pg.365]    [Pg.55]    [Pg.152]    [Pg.364]    [Pg.364]    [Pg.364]    [Pg.365]    [Pg.152]    [Pg.364]    [Pg.364]    [Pg.364]    [Pg.365]    [Pg.55]    [Pg.152]    [Pg.364]    [Pg.364]    [Pg.364]    [Pg.365]    [Pg.257]    [Pg.173]    [Pg.173]    [Pg.175]    [Pg.182]    [Pg.226]    [Pg.672]    [Pg.672]    [Pg.542]    [Pg.308]   
See also in sourсe #XX -- [ Pg.130 ]



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