Answers are grounded in this paper and cite their sources.
Abstract 1) The asymmetric activities of Raney nickel catalysts modified with (+)-2-methylglutamic acid or (+)-2-benzylglutamic acid have been formed to be quite different from that of the catalyst modified with l-glutamic acid. 2) Levorotatory methyl 3-hydroxybutyrate is obtained by the catalyst modified with (+)-2-methylglutamic acid, and the dextrorotatory product by the catalyst modified with (+)-2-benzylglutamic acid. With the catalyst modified with l-glutamic acid, however, the direction of optical rotation of the hydrogenation product is much influenced by the pH and by the temperature of the modifying solution.
No takes yet. Share an insight, caveat, or question.
Izumi et al. (1965) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: