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Journal ArticleDOI

Chemical conversion pathways for carbohydrates

TLDR
A review of the recent developments in liquid phase chemical conversions of monosaccharides, disaccharide, and polysaccharides can be found in this paper, followed by a process-driven approach where the existing carbohydrate conversion pathways are classified according to the types of chemical processes involved.
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This article is published in Green Chemistry.The article was published on 2015-01-01. It has received 271 citations till now.

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Catalytic Transformation of Lignocellulose into Chemicals and Fuel Products in Ionic Liquids

TL;DR: This review focuses on the catalytic chemical conversion of lignocellulose and its primary ingredients into value-added chemicals and fuel products using ILs as the reaction media.
Journal ArticleDOI

Adsorption Behavior of Glucosamine-Based, Pyrimidine-Fused Heterocycles as Green Corrosion Inhibitors for Mild Steel: Experimental and Theoretical Studies

TL;DR: In this article, the effects of electron donating (−CH3 and −OH) and electron withdrawing (−NO2) substituents on the corrosion inhibition efficiency of four glucosamine-based, substituted, pyrimidine-fused heterocycles (CARBs) on mild steel corrosion in 1 M HCl have been investigated using gravimetric, electrochemical, surface morphology (SEM, AFM, and EDX), and computational techniques.
Journal ArticleDOI

Recent advances in hydrodeoxygenation of biomass-derived oxygenates over heterogeneous catalysts

TL;DR: In this paper, the roles of different catalytic sites in Hydrodeoxygenation (HDO) and strategies to stabilize these active sites are discussed, and points to be considered for further research into HDO over heterogeneous catalysts and pending challenges are discussed.
Journal ArticleDOI

Organic Solvent Effects in Biomass Conversion Reactions.

TL;DR: A holistic view of solvent effects, the mechanistic elucidation of these effects, and the careful consideration of the challenges associated with solvent use could assist researchers in choosing and designing improved solvent systems for targeted biomass conversion processes.
Journal ArticleDOI

An overview of biorefinery-derived platform chemicals from a cellulose and hemicellulose biorefinery

TL;DR: This review article provides an overview of the techniques developed for the valorization of biomass in the production of platform chemicals within a biorefinery and the status for commercialization.
References
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Journal ArticleDOI

Telomerization of butadiene with starch under mild conditions.

TL;DR: The design of industrial products based on bioresources is a challenging issue and modification of starch, by hydrophobic chemical substituents, results in an innovativeHydrophobic material through catalytic butadiene telomerization.
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Radiation-induced eco-compatible sulfonated starch/acrylic acid graft copolymers for sucrose hydrolysis

TL;DR: In this article, an ionizing radiation-induced graft-copolymers capable of hosting sulfonic groups and having more effective catalytic activity towards sucrose hydrolysis were prepared.
Journal ArticleDOI

Preparation of Long‐Chain Alkyl D‐Glucosides by Alcoholysis of 1,2:5,6‐Di‐O‐Isopropylidene‐α‐D‐Glucofuranose

TL;DR: The acid-catalysed conversion of 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose (1) in 1-butanol was studied using HPLC, 1HNMR, and 13C NMR.
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Green glycosylation promoted by reusable biomass carbonaceous solid acid: an easy access to β-stereoselective terpene galactosides

TL;DR: An efficient green protocol has been developed for the atom economic glycosylation of unprotected, unactivated Glycosyl donors and glycosYL trichloroacetimidates with the aid of reusable eco-friendly biomass carbonaceous solid acid as catalyst.
Journal ArticleDOI

Eco-friendly preparation of 5-hydroxymethylfurfural from sucrose using ion-exchange resins

TL;DR: In this paper, an efficient preparation of 5-hydroxymethylfurfural from sucrose, a renewable resource, was reported, following a sequence of four steps catalyzed by reusable cation-and anion-exchange resins: hydrolysis, dehydration, glucose/fructose isomerisation and dehydration.
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