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Enantioselective Reformatsky Reaction Using Cinchona Alkaloids as Chiral Ligands
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 Title & Authors
Enantioselective Reformatsky Reaction Using Cinchona Alkaloids as Chiral Ligands
Park, Doo-Han; Choi, Ho-Jin; Lee, Sang-Gi;
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 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;
 Language
English
 Cited by
1.
A Catalytic, Me2Zn-Mediated, Enantioselective Reformatsky Reaction With Ketones, Angewandte Chemie International Edition, 2006, 45, 18, 2951  crossref(new windwow)
2.
A Catalytic, Me2Zn-Mediated, Enantioselective Reformatsky Reaction With Ketones, Angewandte Chemie, 2006, 118, 18, 3017  crossref(new windwow)
3.
An Improved Asymmetric Reformatsky Reaction Mediated by (−)-N,N-Dimethylaminoisoborneol, Organic Letters, 2006, 8, 6, 1125  crossref(new windwow)
4.
A Catalytic Enantioselective Imino-Reformatsky Reaction, Advanced Synthesis & Catalysis, 2006, 348, 15, 2075  crossref(new windwow)
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