ArticleNature communications2025
Producing aryl halides from lignin.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Photocatalytic Lignin Depolymerization and Cross-Coupling With Alcohols to Produce Unsymmetric Aromatic Diols.Angewandte Chemie (International ed. in English) · 2026Article
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Authors and funding
10 authors.
Funding
Abstract
Lignin represents the most abundant biomass resource, which contains aromatic units. Lignin refinery is a promising, sustainable alternative for the production of aromatic chemicals. However, depolymerization and transformation of lignin into aryl halides, which are indispensable chemicals in both the academic and industrial communities, remain challenging. Here, we report a simple and mild method for the depolymerization and halogenation of lignin, leading to the production of useful aryl halides. Notably, hydrogen bond activation for halogenation reagents is essential for substantially increasing the reactivity, resulting a highly efficient cleavage of C-C bonds in lignin. This method is highly selective for breaking C(sp
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Registered trials
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