Chinese Journal of Organic Chemistry >
Enantioselective Hydrosilylation of N-Aryl Diaryl Ketimines
Received date: 2015-12-30
Revised date: 2016-04-02
Online published: 2016-04-07
Supported by
Project supported by the National Natural Science Foundation of China (No. 21172217).
Lewis base catalyzed enantioselective hydrosilylation of non-ortho-substituted N-aryl diaryl ketimines was realized. In the presence of 20 mol% of the optimal catalyst, the reactions provided a series of (diarylmethyl)amines with high yields (up to 97%) in moderate to good enantioselectivities (up to 89% ee). The absolute configuration of one product was determined by X-ray crystallographic analysis.
Key words: diarylmethylamines; diaryl ketimines; chiral Lewis base; hydrosilylation
Hu Xiaoyan , Hu Fangzhi , Zhang Minmin , Liao Yijun , Xu Xiaoying , Yuan Weicheng , Zhang Xiaomei . Enantioselective Hydrosilylation of N-Aryl Diaryl Ketimines[J]. Chinese Journal of Organic Chemistry, 2016 , 36(8) : 1895 -1906 . DOI: 10.6023/cjoc201512049
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