<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(4)</volume><submitter>Miceli M</submitter><pubmed_abstract>The present work aimed to synthesise promising antioxidant compounds as a valuable alternative to the currently expensive and easily degradable molecules that are employed as stabilizers in industrial preparation. Taking into account our experience concerning domino Friedel-Crafts/lactonization reactions, we successfully improved and extended the previously reported methodology toward the synthesis of 3,3-disubstituted-3H-benzofuran-2-one derivatives 9-20 starting from polyphenols 1-6 as substrates and either diethylketomalonate (7) or 3,3,3-trifluoromethyl pyruvate (8) as electrophilic counterpart. The antioxidant capacity of the most stable compounds (9-11 and 15-20) was evaluated by both DPPH assay and Cyclic Voltammetry analyses performed in alcoholic media (methanol) as well as in aprotic solvent (acetonitrile). By comparing the recorded experimental data, a remarkable activity can be attributed to few of the tested lactones.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>E710</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6017620</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis of Benzofuran-2-One Derivatives and Evaluation of Their Antioxidant Capacity by Comparing DPPH Assay and Cyclic Voltammetry.</pubmed_title><pmcid>PMC6017620</pmcid><pubmed_authors>Miceli M</pubmed_authors><pubmed_authors>Rosa P</pubmed_authors><pubmed_authors>Feroci M</pubmed_authors><pubmed_authors>Gasperi T</pubmed_authors><pubmed_authors>Roma E</pubmed_authors><pubmed_authors>Tofani D</pubmed_authors><pubmed_authors>Loreto MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis of Benzofuran-2-One Derivatives and Evaluation of Their Antioxidant Capacity by Comparing DPPH Assay and Cyclic Voltammetry.</name><description>The present work aimed to synthesise promising antioxidant compounds as a valuable alternative to the currently expensive and easily degradable molecules that are employed as stabilizers in industrial preparation. Taking into account our experience concerning domino Friedel-Crafts/lactonization reactions, we successfully improved and extended the previously reported methodology toward the synthesis of 3,3-disubstituted-3H-benzofuran-2-one derivatives 9-20 starting from polyphenols 1-6 as substrates and either diethylketomalonate (7) or 3,3,3-trifluoromethyl pyruvate (8) as electrophilic counterpart. The antioxidant capacity of the most stable compounds (9-11 and 15-20) was evaluated by both DPPH assay and Cyclic Voltammetry analyses performed in alcoholic media (methanol) as well as in aprotic solvent (acetonitrile). By comparing the recorded experimental data, a remarkable activity can be attributed to few of the tested lactones.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-18T15:21:31.096Z</modification><creation>2019-03-27T00:06:37Z</creation></dates><accession>S-EPMC6017620</accession><cross_references><pubmed>29561784</pubmed><doi>10.3390/molecules23040710</doi></cross_references></HashMap>