Stereo-preference in the degradation of the erythro and threo isomers of β-O-4-type lignin model compounds in oxidation processes III: in the reaction with chlorine- and manganese-based oxidants
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biomaterials
Link
http://link.springer.com/article/10.1007/s10086-018-1714-z/fulltext.html
Reference19 articles.
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2. Tsutsumi Y, Kondo R, Imamura H (1993) Reaction of syringylglycerol-β-syringyl ether type of lignin model compounds in alkaline-medium. J Wood Chem Technol 13(1):25–42
3. Criss DL, Elder T, Fisher TH, Schultz TP (2002) Effect of the α-and γ-hydroxyls on the alkaline hydrolysis rate of nonphenolic β-O-4 lignin diastereomers. Holzforschung 56(1):67–72
4. Shimizu S, Yokoyama T, Akiyama T, Matsumoto Y (2012) Reactivity of lignin with different composition of aromatic syringyl/guaiacyl structures and erythro/threo side chain structures in β-O-4 type during alkaline delignification: as a basis for the different degradability of hardwood and softwood lignin. J Agric Food Chem 60(26):6471–6476
5. Shimizu S, Posoknistakul P, Yokoyama T, Matsumoto Y (2013) Quantitative difference in the rates of the β-O-4 bond cleavage between lignin model compounds with and without γ-hydroxymethyl groups during the alkaline pulping process. BioResources 8(3):4312–4322
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