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http://dx.doi.org/10.5012/jkcs.2003.47.6.597

Enantioselective Reformatsky Reaction Using Cinchona Alkaloids as Chiral Ligands  

Park, Doo-Han (Department of Chemistry, Sahmyook University)
Choi, Ho-Jin (Department of Chemistry, Sahmyook University)
Lee, Sang-Gi (Life Sciences Division, Korea Institute of Science and Technology)
Publication Information
Journal of the Korean Chemical Society / v.47, no.6, 2003 , pp. 597-600 More about this Journal
Abstract
Cinchona alkaloids (1-4) were used as chiral ligands for the enantioselective Reformatsky reactions. The order of addition of the Reformatsky reagent to ligands was the important factors for the chiral induction. The ratio of Reformatsky reagent to ligand and aldehyde was also effected on the reaction yields.
Keywords
CInchona Alkaloid; Enantioselective Reformatsky Reaction;
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Times Cited By KSCI : 1  (Citation Analysis)
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