Issue 3, 2016
From the journal:

Organic Chemistry Frontiers

Nickel catalyzed reduction of arenols under mild conditions†

Wen-Juan Shi,a   Xiao-Lei Li,a   Zhao-Wei Lia  and  Zhang-Jie Shi*ab  

* Corresponding authors

a Beijing National Laboratory of Molecular Sciences (BNLMS) and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering and Green Chemistry Center, Peking University, Beijing, China
E-mail: zshi@pku.edu.cn

b State Key Laboratory of Organometallic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Abstract

Nickel catalyzed reduction of arenols has been developed with a mutual activation strategy under mild conditions. The reduction featured a broad substrate scope, non-sensitivity to steric hindrance and no over-reduction of the aromatic rings.

Graphical abstract: Nickel catalyzed reduction of arenols under mild conditions

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Article information

DOI
https://doi.org/10.1039/C5QO00395D
Article type
Research Article
Submitted
24 Nov 2015
Accepted
05 Jan 2016
First published
14 Jan 2016

Org. Chem. Front., 2016,3, 375-379

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Nickel catalyzed reduction of arenols under mild conditions

W. Shi, X. Li, Z. Li and Z. Shi, Org. Chem. Front., 2016, 3, 375 DOI: 10.1039/C5QO00395D

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