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Highly efficient transformation of lignin major segments into quinolines
•A sustainable method to synthesize quinolines from lignin major segments has been successfully developed.•Redox-neutral depolymerization of lignin major segments and construction of quinoline motifs were realized in a one-pot fashion.•A tandem selective cleavage of C-O bonds/dehydrogenation/aza-Mic...
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Published in: | Chemical engineering science 2024-05, Vol.290, p.119899, Article 119899 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | •A sustainable method to synthesize quinolines from lignin major segments has been successfully developed.•Redox-neutral depolymerization of lignin major segments and construction of quinoline motifs were realized in a one-pot fashion.•A tandem selective cleavage of C-O bonds/dehydrogenation/aza-Michael addition/cyclization/dehydration/oxidation sequence is proposed.
The development of a sustainable synthesis route for functional quinolines from lignin β-O-4 segments containing γ-OH group is of high importance to meet biorefinery demands, but remains challenge due to the low cleavage efficiency of this specific motif and the incompatible catalytic systems. In this work a highly efficient transformation of β-O-4 lignin major segments into functional quinolines catalyzed by vanadium-based complex and copper has been developed, obtaining a wide range of substituted quinolines with good yields, which is a two-fold increase of quinolines yields when compared with previous sustainable routes. The pathway of this one-pot cascade reaction is investigated and a potential mechanism is proposed, involving the selective aryl ether cleavage, dehydrogenation, aza-Michael addition, dehydration and oxidation process. This work features a highly efficient transformation of lignin β-O-4 segments into N-heterocyclics without additional an oxidant or reductant agent, providing a concise and sustainable route for functional quinolines synthesis. |
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ISSN: | 0009-2509 1873-4405 |
DOI: | 10.1016/j.ces.2024.119899 |