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Quinoline 1-oxide, hydrogen-exchange

The most reactive position for base-catalyzed hydrogen exchange of the 1-oxide derivatives of quinoline and isoquinoline is the position adjacent to the heteroatom and nearest the fused benzene ring. Thus for isoquinoline 1-oxide the positionalreactivity is given by 1 > >3 > > 4,... [Pg.24]

Yamane et al.[13] determined cobalt in sea water and river waters with a catalytic spectrophotomeiric method after on-line preconcentration using a column packed with quinolin-8-ol immobilized on silica gel. The tartrate eluate from the preconcentraiion had to pass through a second column packed with a strongly acidic cation exchanger to remove iron(III) and manganese(II) which interfere in the catalytic reaction of oxidation of protocatechuic acid by hydrogen peroxide. An extremely low detection limit of 0.005 /ig 1 was obtained. However, the sampling frequency was less than 2 h . ... [Pg.199]


See other pages where Quinoline 1-oxide, hydrogen-exchange is mentioned: [Pg.286]    [Pg.221]    [Pg.300]    [Pg.286]    [Pg.162]    [Pg.365]    [Pg.238]    [Pg.167]    [Pg.97]    [Pg.103]    [Pg.171]    [Pg.232]    [Pg.167]    [Pg.164]    [Pg.53]    [Pg.241]   


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Hydrogen oxidation, exchange

Oxide exchange

Quinoline 1-oxide

Quinoline oxidation

Quinoline, hydrogenation

Quinolines hydrogenation

Quinolines oxidation

Quinolines oxides

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