Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, Hubei, 430079, P. R. China.
Org Biomol Chem. 2012 Feb 28;10(8):1680-5. doi: 10.1039/c1ob06669b. Epub 2012 Jan 5.
A highly practical, catalytic enantioselective cyclic phosphite addition to aldehydes and ketones was developed. The reaction rate of the asymmetric hydrophosphonylation was significantly enhanced by the addition of silver carbonate. Particularly, significant improvement has been achieved on the asymmetric hydrophosphonylation of unactivated ketones, giving quaternary α-hydroxy phosphonates with excellent enantioselectivity (up to 99% ee).
发展了一种高度实用的、催化对映选择性环状亚膦酸酯与醛和酮的加成反应。通过添加碳酸银,不对称氢膦化反应的反应速率得到显著提高。特别是,在未活化酮的不对称氢膦化反应中取得了显著的改进,得到了具有优异对映选择性的季碳α-羟基膦酸酯(高达 99%ee)。