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Enantioselective Aza‐Michael Addition of Imides by Using an Integrated Strategy Involving the Synthesis of a Family of Multifunctional Catalysts,Usage of Multiple Catalysis,and Rational Design of Experiment
Authors:Mattia Silvi  Polyssena Renzi  Deborah Rosato  Cristiana Margarita  Alessio Vecchioni  Ivan Bordacchini  Diego Morra  Alessandro Nicolosi  Riccardo Cari  Dr. Fabio Sciubba  Dr. Daniele M. Scarpino Schietroma  Dr. Marco Bella
Affiliation:1. Department of Chemistry, “Sapienza” University of Roma, P.le Aldo Moro 5, 00185 Roma (Italy);2. Istituto di Chimica Biomolecolare del CNR, P.le Aldo Moro 5, 00185 Roma (Italy)
Abstract:A challenging asymmetric reaction (aza‐Michael addition of imides to enones) has been optimized through an integrated approach involving the synthesis of a family of organocatalysts, multiple catalysis (usage of additives), and finally with rational exploration of the chemical space by the application of the experiment design.
Keywords:asymmetric catalysis  aza‐Michael reaction  enones  imides  synthetic methods
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