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Normal Prismanes

Diphenylcyclopropenone undergoes bimolecular reduction by the action of aluminium amalgam or magnesium-magnesium iodide the product is not, however, the expected pinacol but tetraphenyl-resorcinol [116], It was suggested that a radical anion is the first reduction product and that this then dimerises, as in normal pinacol reductions, but that the dimerisation product rearranges, first to a prismane derivative, then to a bicyclohexadiene derivative, and finally into the resorcinol derivative. [Pg.95]


See other pages where Normal Prismanes is mentioned: [Pg.88]    [Pg.120]    [Pg.936]    [Pg.943]    [Pg.62]    [Pg.48]    [Pg.205]    [Pg.936]    [Pg.943]    [Pg.26]    [Pg.77]    [Pg.193]    [Pg.211]    [Pg.120]    [Pg.157]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.130 ]




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Prismane

Prismanes

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