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
Journal article published in 2013 by
Mattia Silvi,
Polyssena Renzi 
,
Deborah Rosato,
Cristiana Margarita ,
Alessio Vecchioni,
Ivan Bordacchini,
Diego Morra,
Alessandro Nicolosi,
Riccardo Cari,
Fabio Sciubba,
Daniele M. Scarpino Schietroma,
Marco Bella
,
Deborah Rosato,
Cristiana Margarita ,
Alessio Vecchioni,
Ivan Bordacchini,
Diego Morra,
Alessandro Nicolosi,
Riccardo Cari,
Fabio Sciubba,
Daniele M. Scarpino Schietroma,
Marco Bella
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 
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.