Enantioselective hydrogenations of aromatic b-ketoesters 1 and 2
Enantioselective hydrogenation of β-aryl-β-ketoester over α-hydroxy acid-modified Raney nickel catalysts: competitive hydrogenation with methyl acetoacetate
Scheme 1
In the present study, we have extended previous study to obtain further insight into the catalytic behaviors of the enantioselective hydrogenations of aromatic b-ketoesters, represented by 1 and 2 (Scheme 1), through competitive hydrogenations with methyl acetoacetate as a reference substrate over tartaric acid- and malic acid-modiļ¬ed Raney nickel catalysts.
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