Furans represent one of the most important classes of intermediates in the conversion of non-edible lignocellulosic biomass into bio-based chemicals and fuels. At present, bio-furan derivatives are generally obtained from cellulose and hemicellulose fractions of biomass via the acid-catalyzed dehydration of their relative C6–C5 sugars and then converted into a wide range of products. Furfural (FUR) and 5-hydroxymethylfurfural (HMF) are surely the most used furan-based feedstocks since their chemical structure allows the preparation of various high-value-added chemicals. Among several well-established catalytic approaches, hydrogenation and oxygenation processes have been efficiently adopted for upgrading furans; however, harsh reaction conditions are generally required. In this review, we aim to discuss the conversion of biomass derived FUR and HMF through unconventional (transfer hydrogenation, photocatalytic and electrocatalytic) catalytic processes promoted by heterogeneous catalytic systems. The reaction conditions adopted, the chemical nature and the physico-chemical properties of the most employed heterogeneous systems in enhancing the catalytic activity and in driving the selectivity to desired products are presented and compared. At the same time, the latest results in the production of FUR and HMF through novel environmental friendly processes starting from lignocellulose as well as from wastes and by-products obtained in the processing of biomass are also overviewed.

The aim of this tutorial review is to provide a general overview of processes, technologies and challenges in the production of pharmaceutical and bioactive compounds from food waste and lignocellulosic residues.

The catalytic transfer hydrogenolysis (CTH) of benzyl phenyl ether has been investigated using Pd/Fe₃O₄ as a heterogeneous catalyst and 2-propanol as a H-donor. After 90 minutes at 240 °C, the cleavage of the ester C–O bond occurs as the only reaction route, whereas hydrogenation of the aromatic ring was not observed.

Lignocellulosic biomasses have a tremendous potential to cover the future demand of bio-based chemicals and materials, breaking down our historical dependence on petroleum resources. The development of green chemical technologies, together with the appropriate eco-politics, can make a decisive contribution to a cheap and effective conversion of lignocellulosic feedstocks into sustainable and renewable chemical building blocks. In this regard, the use of an indirect H-source for reducing the oxygen content in lignocellulosic biomasses and in their derived platform molecules is receiving increasing attention. In this contribution we highlight recent advances in the transfer hydrogenolysis of cellulose, hemicellulose, lignin, and of their derived model molecules promoted by heterogeneous catalysts for the sustainable production of biofuels and biochemicals.

The use of lignocellulosic biomasses for the production of renewable hydrogen is surely among the hot-topic research tasks. In this review, we report on the recent advances in the catalytic conversion of cellulose and its derived C6-C5 sugars (glucose, fructose, and xylose) and polyols (sorbitol and xylitol) into hydrogen via aqueous phase reforming (APR) reactions. The APR processes are considered to be new sustainable catalytic routes for converting the carbohydrate fraction of biomasses into hydrogen at milder reaction conditions if compared with the traditional reforming reactions. Particular emphasis is given to the development of new and active catalysts and to the optimization of reaction conditions that aimed to maximize hydrogen production with a low concentration of CO avoiding, at the same time, the formation of alkanes.