<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(40)</volume><submitter>Soliman AIA</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Assiut University</funding><funding>Zhejiang University</funding><funding>Canada Research Chairs</funding><pubmed_abstract>Knoevenagel condensation is a chemical reaction between aldehydes and active methylene-containing compounds in the presence of heterogeneous, basic homogenous organic or inorganic catalysts and solvent or neat systems. Herein, we introduced a new strategy for this synthesis by using the aqueous solution of cationic kraft lignin (CKL) as a catalyst. The CKL was synthesized through the reaction of kraft lignin (KL) with glycidyltrimethylammonium chloride (GTMAC) in a basic medium. The optimal reaction conditions for the Knoevenagel reaction were 5% catalyst load (weight of catalyst to the weight of benzaldehyde), water as the solvent, and at room temperature, which generated the products with a yield of 97%, illustrating that the CKL was an effective homogenous and green catalyst. The result</pubmed_abstract><journal>RSC advances</journal><pagination>29595-29605</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11409447</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cationic lignin as an efficient and sustainable homogenous catalyst for aqueous Knoevenagel condensation reactions.</pubmed_title><pmcid>PMC11409447</pmcid><pubmed_authors>Bacchus A</pubmed_authors><pubmed_authors>Soliman AIA</pubmed_authors><pubmed_authors>Zare R</pubmed_authors><pubmed_authors>Fatehi P</pubmed_authors><pubmed_authors>Sutradhar S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cationic lignin as an efficient and sustainable homogenous catalyst for aqueous Knoevenagel condensation reactions.</name><description>Knoevenagel condensation is a chemical reaction between aldehydes and active methylene-containing compounds in the presence of heterogeneous, basic homogenous organic or inorganic catalysts and solvent or neat systems. Herein, we introduced a new strategy for this synthesis by using the aqueous solution of cationic kraft lignin (CKL) as a catalyst. The CKL was synthesized through the reaction of kraft lignin (KL) with glycidyltrimethylammonium chloride (GTMAC) in a basic medium. The optimal reaction conditions for the Knoevenagel reaction were 5% catalyst load (weight of catalyst to the weight of benzaldehyde), water as the solvent, and at room temperature, which generated the products with a yield of 97%, illustrating that the CKL was an effective homogenous and green catalyst. The result</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2025-04-06T12:52:18.792Z</modification><creation>2025-04-06T12:52:18.792Z</creation></dates><accession>S-EPMC11409447</accession><cross_references><pubmed>39297031</pubmed><doi>10.1039/d4ra05763e</doi></cross_references></HashMap>