Chemistry Letters p. 1257 - 1258 (1998)
Update date:2022-08-24
Topics:
Nakagawa, Satoshi
Sugimura, Takashi
Tai, Akira
A comparative study of the reactivities of the hydrogenation of β-ketoesters over tartaric acid-modified and unmodified Raney nickels indicated that a substrate specific activation by the tartaric acid modification is the reason for the almost perfect enantio-differentiation in the reaction of methyl 3-cyclopropyl-3-oxopropanoate (4).
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