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Methyl hydrogen succinate, hydrolysis

The methanol obtained from the acid hydrolysis of methyl hydrogen succinate in water containing O18 contained none of the heavy isotope 7... [Pg.227]

The ring structure of the ribose residue was ascertained" in the same general manner as for adenosine and guanosine. Triacetyl-dihydrouridine was prepared by the hydrogenation of triacetyl-uridine. On simultaneous deacetylation and methylation this was transformed to the fully methylated dihydro-uridine. By simultaneous hydrolysis and oxidation of this product, with hydrobromic acid and bromine, trimethyl -D-ribonolactone was formed, its identity being confirmed by oxidation to meso-dimethoxy-succinic acid. It follows that the ribose component has the furanose ring structure, and that uridine is 3 -D-ribofuranosyl-uracil. [Pg.209]

Succinic anhydride, 41, 158, 283 o ,/3-bis(triphenyl methyl), MA in synthesis, 198 p-carboxymethylbenzyl, MA in synthesis, 202 commercial preparation, 41, 42 conversion to A2-car boxy anhydride, 225 1,3-dihydronaphthlene substituted, 198 hydrolysis rate, 73, 74 indane substituted, 198 MA hydrogenation product, 236 phosphine reaction, 229 preparation, 15... [Pg.866]


See other pages where Methyl hydrogen succinate, hydrolysis is mentioned: [Pg.104]    [Pg.175]    [Pg.468]    [Pg.1288]    [Pg.199]   
See also in sourсe #XX -- [ Pg.104 ]




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