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.

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

Polyssena Renzi;
2013-01-01

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.
2013
19
30
9973
9978
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201301493
aza-michael reaction; imides; synthetic methods; enones; asymmetric catalysis
Mattia Silvi; Polyssena Renzi; Deborah Rosato; Chiara Margarita; Alessio Vecchioni; Ivan Bordacchini; Diego Morra; Alessandro Nicolosi; Riccardo Cari; Fabio Sciubba; Daniele Maria Scarpino Schietroma; Marco Bella
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1729116
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