A wide variety of commodity chemicals can be produced from the catalytic oxidation of carbohydrates or carbohydrate derived molecules including formic acid, acetic acid, glycolic acid, gluconic acid, glucaric acid, malonic acid, oxalic acid, 2,5-diformylfuran (DFF), 5-hydroxymethyl-2-furancarboxylic acid (HFCA), 5-formyl-2-furancarboxylic acid (FFCA), and 2,5-furandicarboxylic acid (FDCA). This review will highlight the recent research progress in the development of new routes for the production of organic acids and furan compounds via catalytic oxidation reactions. Particular attention will be paid to these one-pot reactions with the requirements of an acidic site and a metal site. For the one-pot transformation of cellobiose or lignocellulose into gluconic acid, these reactions were performed via a one-step strategy using a single catalyst containing an acidic site and a metal site. However, a two-step strategy was adopted for the oxidative transformation of carbohydrates into DFF or FDCA in order to avoid the oxidation of the carbohydrates. The first step was performed for the dehydration of carbohydrates into 5-hydroxylmethylfuran (HMF) in the presence of an acid catalyst, and the second step was performed for the oxidation of HMF into DFF or FDCA with a metal catalyst.

The cobalt–nitrogen catalyst shows high activity for selective reduction of nitro compounds with H ₂ and other hydrogen donors.

A new method for the selective aerobic oxidation of 5-hydroxymethylfurfural (HMF) into 2,5-furandicarboxylic acid (FDCA) has been developed employing a magnetically separable [γ-Fe₂O₃@HAP-Pd(0)] catalyst. The catalyst was prepared by the exchange of Pd²⁺ with Ca²⁺ in γ-Fe₂O₃@HAP, followed by reduction of the Pd²⁺ to Pd(0) nanoparticles, and well characterized by TEM, XRD and XPS. The catalyst showed high activity in the oxidation of HMF to FDCA in water, with 97% HMF conversion and a 92.9% yield of FDCA under optimal reaction conditions. The method developed has demonstrated some advantages, including its sole requirement of a stoichiometric base, and high catalytic performance under atmospheric oxygen, even in air. More importantly, the γ-Fe₂O₃@HAP-Pd(0) catalyst was readily separated from the reaction solution using an external magnetic field and was successfully reused during five consecutive reaction runs while retaining its catalytic effectiveness. This study provides a green and sustainable method for the production of valuable chemicals from renewable resources.

Selective hydrogenolysis of the C_aryl–O bonds in lignin is a key strategy for the generation of fuels and chemical feedstocks from biomass. Currently, hydrogenolysis has been mainly conducted using hydrogen, which is flammable and not sustainable or economical. Herein, an external hydrogen-free process for aryl ethers hydrogenolysis in lignin models and dioxasolv lignin over nickel nanoparticles supported on Al₂O₃, is reported. Kinetic studies reveal that the transfer hydrogenolysis activity of the three model compounds decreased in the following order: benzyl phenyl ether (α-O-4), 2-phenylethyl phenyl ether (β-O-4) and diphenyl ether (4-O-5), which linearly corresponds to their binding energies and the activation energies. The main reaction route for the three model compounds was the cleavage of the ether bonds to produce aromatic alkanes and phenol, and the latter was further reduced to cyclohexanol. Dioxasolv lignin depolymerization results exhibit a significant C_aryl–O decrease over the Ni nanoparticles supported on Al₂O₃ with iso-propanol as the hydrogen source through 2D-HSQC-NMR analysis, which confirmed the transfer hydrogenolysis conclusion in the model study. This work provides an economical and environmentally-friendly method for the selective cleavage of lignin and lignin model compounds into value-added chemicals.