Nickel catalyzed reduction of arenols under mild conditions
Literature Information
Publication Date
2016-01-14
DOI
10.1039/C5QO00395D
Impact Factor
5.281
Authors
Wen-Juan Shi, Xiao-Lei Li, Zhao-Wei Li
View Original
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.
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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
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