Revisiting the mechanism of β - O -4 bond cleavage during acidolysis of lignin. Part 9: Comprehensive results for guaiacyl-type compounds and the difference in participation mode of bromide and chloride anions between C 6 -C 3 -type and C 6 -C 2 -type compounds-Reference-Cited by-同舟云学术

Revisiting the mechanism of β - O -4 bond cleavage during acidolysis of lignin. Part 9: Comprehensive results for guaiacyl-type compounds and the difference in participation mode of bromide and chloride anions between C ₆ -C ₃ -type and C ₆ -C ₂ -type compounds

Published:2024-02-17 Issue:3 Volume:44 Page:147-163
ISSN:0277-3813
Container-title:Journal of Wood Chemistry and Technology
language:en
Short-container-title:Journal of Wood Chemistry and Technology

Author:

Ye Qiaoqiao¹,Katsumata Kyoko S.¹,Komatsu Toshihiro¹,Yokoyama Tomoya¹

Affiliation:

1. Laboratory of Wood Chemistry, Department of Biomaterial Sciences, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan

Funder

Japan Society for the Promotion of Science [JSPS KAKENHI

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/02773813.2024.2314477

Reference30 articles.

1. Structural and Molecular Properties of Residual Birch Kraft Lignins

2. Action of Mineral Acid on Lignin and Model Substances of Guaiacylglycerol-β-aryl Ether Type

3. Isolation of 3-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-2-propanone from Lignin.

4. Spectrochemical Estimation of Phenylcoumaran Elements in Lignin.

5. On the Separation of Lignin Degradation Products.

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1. Revisiting the mechanism of β-O-4 bond cleavage during acidolysis of lignin part 10: reactions of C6–C2-type non-phenolic syringyl model compounds and comparison of the reactions with those of the guaiacyl analogues;Journal of Wood Science;2024-05-18