From structural obstacle to tailored bisphenols: The condensation revolution in lignin valorization
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REFERENCES
[1] Lan W., Amiri M.T. and Hunston C.M. et al. (2018). Protection group effects during α,γ-diol lignin stabilization promote high-selectivity monomer production. Angew. Chem. Int. Ed. 57:1356−1360. DOI:10.1002/anie.201710838 [2] Rahimi A., Ulbrich A. and Coon J.J. et al. (2014). Formic-acid-induced depolymerization of oxidized lignin to aromatics. Nature 515:249−252. DOI:10.1038/nature13867 [3] Gong Z., Yang G. and Huang L. et al. (2023). Phenol-assisted depolymerisation of condensed lignins to mono-/poly-phenols and bisphenols. Chem. Eng. J. 455:140628. DOI:10.1016/j.cej.2022.140628 [4] Li N., Yan K. and Rukkijakan T. et al. (2024). Selective lignin arylation for biomass fractionation and benign bisphenols. Nature 630:381−386. DOI:10.1038/s41586-024-07446-5 [5] Huang L., Zhao C. and Gong Z. et al. (2025). Manipulation of lignin condensation pathways to produce different bisphenols from biomass. The Innovation 6:100997. DOI:10.1016/j.xinn.2025.100997 -
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Fu X., Xiao L. and Sun R. (2025). From structural obstacle to tailored bisphenols: The condensation revolution in lignin valorization. The Innovation Materials 3:100172. https://doi.org/10.59717/j.xinn-mater.2025.100172
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Fu X., Xiao L. and Sun R. (2025). From structural obstacle to tailored bisphenols: The condensation revolution in lignin valorization. The Innovation Materials 3:100172. https://doi.org/10.59717/j.xinn-mater.2025.100172
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Figure 1.
Pathways for synthesizing bisphenol P3 from lignin
