화학공학소재연구정보센터
Journal of Molecular Catalysis A-Chemical, Vol.393, 171-174, 2014
Enantioselective 1,3-dipolar cycloadditions of nitrones with unsaturated aldehydes promoted by a recyclable tetraarylphosphonium supported imidazolidinone catalyst
The tetraarylphosphonium supported chiral imidazolidinone catalyzes the enantioselective 1,3-dipolar cycloadditions of nitrones and alpha,beta-unsaturated aldehydes to provide isoxazolidine aldehydes in good yields with excellent diastereo- and enantioselectivities. Most importantly, the tetraarylphosphonium supported imidazolidinone catalyst can be readily recovered and recycled for further transformations at least four cycles without observing significant decrease in yield and stereoselectivity. (C) 2014 Elsevier B.V. All rights reserved.