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Asymmetric Michael addition reactions of pyrrolones with chalcones catalyzed by vicinal primary-diamine salts†
Xiaolei Du,Dawei Yin,Zemei Ge,Xin Wang,Runtao Li
RSC Advances Pub Date : 05/05/2017 00:00:00 , DOI:10.1039/C7RA03069J
Abstract

The efficient asymmetric Michael addition reactions of pyrrolones with chalcones catalyzed by a simple and commercially available chiral 1,2-diaminocyclohexane-2-(N-Boc-amino)benzoic acid have been developed to provide the corresponding Michael adducts in good yields (up to 90%) and high enantioselectivities (up to 95% ee).

Graphical abstract: Asymmetric Michael addition reactions of pyrrolones with chalcones catalyzed by vicinal primary-diamine salts
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