I. Scheme, 1: Schematic representation of the lignin sulfonation

I. Scheme, 2: Schematic representation of lignin copolymerization with lactide 48

I. Scheme, Mechanism of stabilizing radicals by tetralin

I. I. Scheme, 1: Acetylation of hydroxyl groups in lignin

I. I. Scheme, Reaction of tag hydroxyls presented in lignin with 2-chloro-4,4, vol.2, pp.5-6

I. V. Scheme, 1: Reaction scheme A of lignin hydroconversion

I. V. Scheme, 2: Reaction scheme of decarboxylation

I. V. Scheme, 3: Reaction scheme of demethylation and demethoxylation of -OCH3

I. V. Scheme, 4: Reaction scheme B of lignin hydroconversion

I. V. Scheme, 5: Breakup of ether bonds and creating of free phenolics OH

I. V. Scheme, Methyl-substitution reaction due to a heterolytic cleavage of -OCH3 bond, vol.6

I. V. Scheme, 7: Reaction scheme C of lignin hydroconversion

I. V. Scheme, Reaction scheme D of lignin hydroconversion, vol.8

I. V. Scheme, Conversion of cutin-like moieties to long-chain alkanes, vol.9

I. V. Scheme, 10: Transformation of methoxy-substituted phenols to alkylphenols

I. V. Scheme, 11: Conversion of the ferulic acid ester into 4-ethylphenol

I. V. Scheme, 12: Conversion of benzofurane entities into 2-ethylphenol

I. V. Scheme, 13: Reaction scheme for hydrodeoxygenation of alkylphenols

I. V. Scheme, 14: General depolymerization of lignin

I. V. Scheme, 15: Transformation of monomers in the liquid phase

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