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Hydrogenation catalyst, Adams’ platinic

Forsyth et al. found that gelsemicine contains three active hydrogen atoms (Zerewitinov determination), yields a non-basic, monobenzoyl derivative, m.p. 232°, and behaves as a secondary base giving JV-methyl-gelsemicine hydriodide, m.p. 227°, on treatment with methyl iodide. It does not react with either hydroxylamine or 2 4-dinitrophenylhydrazine. On hydrogenation in dry acetic acid in presence of Adams s platinic oxide catalyst it absorbs three molecules of hydrogen. [Pg.739]

Also obtained by catalytic hydrogenation of 7-acetyl-4,6-dihydroxy-2-isoprope-nylcoumaran in the presence of platinic oxide (Adams catalyst) in methanol (72%) [2847]. [Pg.961]

Krupp and others [204] proposed that skeletal platinum, prepared by decomposition of an alloy between platinum and aluminum, should be used as catalyst. As shown by Petrii and Marvet [209], hydrogen adsorption isotheims for disperse platinum catalysts (platinized platinum, platinum Idack, Adams platinum, and various forms of skeletal platinum) in aqueous solutions of electrolytes exhibit relatively small differences. [Pg.359]


See other pages where Hydrogenation catalyst, Adams’ platinic is mentioned: [Pg.25]    [Pg.17]    [Pg.3]    [Pg.40]    [Pg.191]    [Pg.738]    [Pg.904]    [Pg.448]    [Pg.32]    [Pg.380]    [Pg.426]    [Pg.520]   


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ADaM

Adams catalyst

Adams hydrogenation

Adams’ catalyst hydrogenation

Hydrogenation catalyst, Adams’ platinic oxide

Platinate

Platination

Platinic

Platinization

Platinized

Platinizing

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