Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones

41Citations
Citations of this article
22Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

We disclose the synthesis of a series of manganese complexes of chiral iminopyridine oxazoline ligands and their application in the first manganese-catalyzed asymmetric ketone hydrosilylations. The most sterically hindered manganese catalyst bearing two CH(Ph)2 groups at the 2,6-ortho positions of the imino aryl ring and a tBu group on the oxazoline ring furnishes the secondary alcohols in high enantioselectivities and yields.

Cite

CITATION STYLE

APA

Ma, X., Zuo, Z., Liu, G., & Huang, Z. (2017). Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones. ACS Omega, 2(8), 4688–4692. https://doi.org/10.1021/acsomega.7b00713

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free