Selective Hydrodeoxygenation for the Synthesis of Oxygen-Containing Chemicals: Fossil-Based Substrates to Biomass-Based Ones

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ID: 314194
2026
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Abstract
Abstract Hydrodeoxygenation of oxygen-containing aliphatic compounds has emerged together with the concept of biomass refinery. The hydrogenolysis of C-O bond is a useful and central reaction for hydrodeoxygenation. There are two different approaches in C-O hydrogenolysis: indirect multi step method (dehydrogenation-dehydration-hydrogenation and dehydration-hydrogenation routes) and direct C-O scission. The indirect route proceeds on conventional catalysts for C-O hydrogenolysis such as Ru- and Cu-based ones. The catalysts for the direct C-O hydrogenolysis have been recently developed. In this review, the key to controlling selectivity in hydrogenolysis of sterically hindered and unhindered C-O bonds has been described in the cases of glycerol, erythritol, and 1,4-anhydroerythritol.
Reference Key
openalex_W7161828203 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Keiichi Tomishige, Mizuho Yabushita, Yoshinao Nakagawa
Journal bulletin of the chemical society of japan
Year 2026
DOI
10.1093/bulcsj/uoag063
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