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Recyclable cinchona alkaloid catalyzed asymmetric Michael addition reaction
Authors:Xin Huang  Wen-Bin YiDanash Ahad  Wei Zhang
Affiliation:Department of Chemistry, University of Massachusetts Boston, 100 Morrissey Boulevard, Boston, MA 02125, USA
Abstract:A highly enantioselective and diastereoselective Michael addition reaction of α-fluoro-β-ketoesters with maleimides is catalyzed by fluorous cinchona alkaloid to afford two adjacent chiral centers. The catalyst attached with a perfluroalkyl tag can be recovered by fluorous solid-phase extraction (F-SPE).
Keywords:Organocatalysis   Asymmetric synthesis   Cinchona alkaloid   Fluorous   Michael addition
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