화학공학소재연구정보센터
Reaction Kinetics and Catalysis Letters, Vol.93, No.1, 75-83, 2008
Asymmetric synthesis of alpha-aryloxy alcohols via kinetic resolution of terminal epoxides catalyzed by (R,R)-N,N'-bis(2-hydroxy-5-tert-butylsalisilidine)-1,2-cyclohexenediamino cobalt
New chiral Co-salen complexes with tert-butyl group in position 5 of the aromatic ring in the structure have been synthesized and they were applied as a chiral catalyst. A dimeric chiral salen having a transition metal salt such as AlCl3, displayed very high catalytic reactivity and enantioselectivity for the asymmetric ring opening of epoxides to synthesize optically pure alpha-aryloxy alcohols via phenolic kinetic resolution.