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Issue 66, 2020
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Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst

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Abstract

The selective hydrodeoxygenation of hydroxyacetophenone derivatives is achieved opening a versatile pathway for the production of valuable substituted ethylphenols from readily available substrates. Bimetallic iron ruthenium nanoparticles immobilized on an imidazolium-based supported ionic liquid phase (Fe25Ru75@SILP) show high activity and stability for a broad range of substrates without acidic co-catalysts.

Graphical abstract: Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst

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Supplementary files

Article information


Submitted
25 May 2020
Accepted
13 Jul 2020
First published
16 Jul 2020

This article is Open Access

Chem. Commun., 2020,56, 9509-9512
Article type
Communication

Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst

L. Goclik, L. Offner-Marko, A. Bordet and W. Leitner, Chem. Commun., 2020, 56, 9509
DOI: 10.1039/D0CC03695A

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