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Chiral, polysubstituted proline esters, obtained via cycloaddition reactions   of azomethine ylides, have been studied as organocatalysts in Michael   reaction of aldehydes/ketones and vinylsulphones. Under optimised reaction   conditions employing 10 mol% of the catalyst in wet CH2Cl2 yields of the   products were generally good while the enantioselectivity varied reaching up   to 52%. [Projekat Ministarstva nauke Republike Srbije, br. 172009

Substituted proline derivatives as organocatalysts in Michael reaction