Effects of aromatic ring type on reactions subsequent to the β-O-4 bond cleavage of non-phenolic lignin model compounds under alkaline pulping conditions
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Springer Science and Business Media LLC
Subject
Biomaterials
Link
http://link.springer.com/article/10.1007/s10086-018-1739-3/fulltext.html
Reference26 articles.
1. Hughes GK, Thompson EOP (1949) Studies in the demethylation of thioanisole. J Proc R Soc N S W 83:269–272
2. Gierer J, Kunze I (1961) Cleavage of β-hydroxyalkyl ary ethers by alkali (in German). Acta Chem Scand 15:803–807
3. Gierer J, Noren I (1962) Reactions of lignin on sulfate digestion II: Model experiments on the cleavage of aryl alkyl ethers by alkali (in German). Acta Chem Scand 16:1713–1729
4. Gierer J, Noren I (1962) Cleavage of β-hydroxyalkyl ary ethers by alkali II: the stereochemical course (in German). Acta Chem Scand 16:1976–1988
5. Gierer J, Lenz B (1965) Reactions of lignin during sulphate cooking Part 6: formation of 1,2-glycol groups in milled wood lignin on treatment with 2 N sodium hydroxide at 170 °C. Svensk Papperstidn 68:334–338
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