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Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones.


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.

SUBMITTER: Ma X 

PROVIDER: S-EPMC6641774 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones.

Ma Xiaochen X   Zuo Ziqing Z   Liu Guixia G   Huang Zheng Z  

ACS omega 20170818 8


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)<sub>2</sub> groups at the 2,6-ortho positions of the imino aryl ring and a <i>t</i>Bu group on the oxazoline ring furnishes the secondary alcohols in high enantioselectivities and yields. ...[more]

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