College of Chemical Engineering, Zhejiang University of Technology , Hangzhou 310014, China.
J Am Chem Soc. 2016 Apr 27;138(16):5198-201. doi: 10.1021/jacs.6b01214. Epub 2016 Apr 19.
A highly enantioselective palladium/l-proline-catalyzed α-arylative desymmetrization of cyclohexanones was developed. The new strategy for α-arylation reaction led to a series of optically active morphan derivatives bearing α-carbonyl tertiary stereocenters in good yields with excellent enantioselectivities (up to 99% ee).
发展了一种高对映选择性钯/l-脯氨酸催化的环己酮的α-芳基去对称化反应。这种新的α-芳基化反应策略得到了一系列光学活性的吗啡衍生物,它们带有α-羰基三级立体中心,产率高,对映选择性好(高达 99%ee)。