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Thiophene acid-catalyzed hydrogen exchange

Acid-catalyzed hydrogen exchange is used as a measure of the comparative reactivity of different aromatic rings (see Table 5). These reactions take place on the neutral molecules or, at high acidities, on the cations. At the preferred positions the neutral isoxazole, isothiazole and pyrazole rings are all considerably more reactive than benzene. Although the 4-position of isothiazole is somewhat less reactive than the 4-position in thiophene, a similar situation does not exist with isoxazole-furan ring systems. [Pg.57]

Relative Rates of 2-Substitution of Thiophenes RC4HjS in Acid-Catalyzed Hydrogen Exchange... [Pg.88]


See other pages where Thiophene acid-catalyzed hydrogen exchange is mentioned: [Pg.307]    [Pg.184]    [Pg.212]    [Pg.399]    [Pg.399]    [Pg.501]    [Pg.771]    [Pg.771]    [Pg.185]    [Pg.185]    [Pg.90]    [Pg.522]   
See also in sourсe #XX -- [ Pg.307 ]




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Acid-catalyzed hydrogen exchange

Acidity exchange

Exchangeable acidity

Hydrogen acid catalyzed

Hydrogen catalyzed

Hydrogenation, catalyzed

Thiophene, hydrogenation

Thiophenes hydrogenation

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