Issue 19, 2013

Synthesis of a series of novel chiral Lewis base catalysts and their application in promoting asymmetric hydrosilylation of β-enamino esters

Abstract

A series of novel chiral Lewis base catalysts were synthesized from L-serine and applied in the hydrosilylation of β-enamino esters, in which the optimal one promoted the reactions to afford a wide variety of β-amino esters in good yields with good enantioselectivities. It is noteworthy that several cyclic substrates were hydrosilylated under the optimal conditions to give the cyclic β-amino esters with high yields, good diastereoselectivities as well as good ee values.

Graphical abstract: Synthesis of a series of novel chiral Lewis base catalysts and their application in promoting asymmetric hydrosilylation of β-enamino esters

Supplementary files

Article information

Article type
Communication
Submitted
01 Mar 2013
Accepted
22 Mar 2013
First published
27 Mar 2013

Org. Biomol. Chem., 2013,11, 3089-3093

Synthesis of a series of novel chiral Lewis base catalysts and their application in promoting asymmetric hydrosilylation of β-enamino esters

X. Chen, X. Hu, C. Shu, Y. Zhang, Y. Zheng, Y. Jiang, W. Yuan, B. Liu and X. Zhang, Org. Biomol. Chem., 2013, 11, 3089 DOI: 10.1039/C3OB40430G

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