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UDCA was synthesized in a divided electrolytic cell by direct electroreduction of 7K-LCA.
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Reduction elimination of acetylated thioxylopyranosyl bromide or acetylated thioxylopyranosyl chloride affording thioxylal is easily performed by direct electroreduction or using niobocene dichloride as catalyst.
In addition, due to the peculiar structure of Fc@DWNTs, direct electroreduction of oxidation product of DA was also observed.
A new kind of electrolyte composed of molten fluorides has been evaluated in order to perform a feasibility study of the direct electroreduction reaction.
The electroreduction process involves at least the electroreduction of an inner relatively thin oxide layer followed by the electroreduction of an outer thick hydrous gold oxide layer.
By the electroreduction of CO2, the main products were formic acid and carbon monoxide.
When the protonation reaction is slow compared to the cleavage reaction, a direct method of electroreduction of ketones to hydrocarbons, through the intermediate alcohol, can be proposed.
Electrosynthesis of glyoxylic acid by electroreduction of oxalic acid has long been well known.
In our previous work, ursodeoxycholic acid was prepared by electroreduction of 7-ketolithocholic acid.
In this electrochemical reaction, ursodeoxycholic acid was synthesized by electroreduction of 7-ketolithocholic acid under certain conditions.
In our previous work, UDCA was prepared by electroreduction of 7-ketolithocholic acid (3α-hydroxy-7-oxo-5β-cholanic acid, 7K-LCA) [[9]].
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