<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Arafa WAA</submitter><funding>Al Jouf University</funding><pagination>5114</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11547704</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(21)</volume><pubmed_abstract>Our novel binuclear complex-anchored Ru(III) catalyst, designed and assembled by sonicating 2,2'-(4,6-dihydroxy-1,3-phenylene)bis(1&lt;i>H&lt;/i>-benzo[&lt;i>d&lt;/i>]imidazole-4-carboxylic acid), Ru(DMSO)&lt;sub>4&lt;/sub>Cl&lt;sub>2&lt;/sub> and 4-methylpyridine, demonstrates remarkable efficiency and selectivity. It promotes one-pot reactions, including active methylenes and benzyl alcohols in water, via a tandem aerobic oxidation/Knoevenagel condensation process, yielding benzylidene malononitrile in excellent yields. The catalyst's ability to oxidize benzyl alcohols to aldehydes, which then undergo Knoevenagel condensation with active methylenes, makes it a multifunctional catalyst. Notably, the catalyst can be successfully retrieved and recycled for five successive rounds with no significant decrease in cat</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>A Ru-Based Complex for Sustainable One-Pot Tandem Aerobic Oxidation-Knoevenagel Condensation Reactions.</pubmed_title><pmcid>PMC11547704</pmcid><funding_grant_id>DGSSR-2023-02-02344</funding_grant_id><pubmed_authors>Arafa WAA</pubmed_authors><pubmed_authors>Mourad AK</pubmed_authors><pubmed_authors>Brase S</pubmed_authors><pubmed_authors>Nayl AA</pubmed_authors><pubmed_authors>Youssef AMS</pubmed_authors><pubmed_authors>Ahmed IM</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Ru-Based Complex for Sustainable One-Pot Tandem Aerobic Oxidation-Knoevenagel Condensation Reactions.</name><description>Our novel binuclear complex-anchored Ru(III) catalyst, designed and assembled by sonicating 2,2'-(4,6-dihydroxy-1,3-phenylene)bis(1&lt;i>H&lt;/i>-benzo[&lt;i>d&lt;/i>]imidazole-4-carboxylic acid), Ru(DMSO)&lt;sub>4&lt;/sub>Cl&lt;sub>2&lt;/sub> and 4-methylpyridine, demonstrates remarkable efficiency and selectivity. It promotes one-pot reactions, including active methylenes and benzyl alcohols in water, via a tandem aerobic oxidation/Knoevenagel condensation process, yielding benzylidene malononitrile in excellent yields. The catalyst's ability to oxidize benzyl alcohols to aldehydes, which then undergo Knoevenagel condensation with active methylenes, makes it a multifunctional catalyst. Notably, the catalyst can be successfully retrieved and recycled for five successive rounds with no significant decrease in cat</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-07-09T13:25:13.835Z</modification><creation>2025-04-04T00:38:37.664Z</creation></dates><accession>S-EPMC11547704</accession><cross_references><pubmed>39519755</pubmed><doi>10.3390/molecules29215114</doi></cross_references></HashMap>