Asymmetric hydrogenation of imines with chiral alkene-derived boron Lewis acids
Xiaoqin Liu1, Ting Liu, Wei Meng
1Beijing National Laboratory of Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China. mengwei@iccas.ac.cn haifengdu@iccas.ac.cn.
Abstract:
With the aim of developing easily accessible chiral Lewis acids for asymmetric hydrogenation, a variety of binaphthyl-based chiral alkenes were prepared in one step from the corresponding diols. Using the in situ generated chiral boron Lewis acids through the hydroboration of chiral alkenes with Piers' borane, metal-free asymmetric hydrogenations of imines were realized to furnish the desired amine products in high yields with up to 89% ee.
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