<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brito JM</submitter><funding>Fundação de Apoio a Pesquisa do Estado de Goiás</funding><funding>Coordenação de Aperfeicoamento de Pessoal de Nível Superior</funding><funding>Universidade Federal de Mato Grosso do Sul</funding><funding>National Council for Scientific and Technological Development</funding><pagination>391</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12844472</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(2)</volume><pubmed_abstract>Herein, we disclose a highly efficient pathway toward 3-selenylated chromone derivatives via electrosynthesis domino C(sp&lt;sup>2&lt;/sup>)-H bond selenylation/cyclization/deamination of 2-hydroxyaryl enaminones with diselenides. This method showed mild conditions, easy operation, a wide substrate scope, and good functional group tolerance. Furthermore, this electrosynthesis strategy was amenable to scaling up the reaction. Additionally, the preliminary experiments revealed that this reaction probably proceeded via a cation pathway instead of a radical pathway.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Electrochemical Synthesis of 3-Selenyl-Chromones via Domino C(sp&lt;sup>2&lt;/sup>)-H Bond Selenylation/Annulation of Enaminones.</pubmed_title><pmcid>PMC12844472</pmcid><funding_grant_id>309975/2022-0</funding_grant_id><funding_grant_id>001</funding_grant_id><funding_grant_id>Chamada Pública FAPEG N° 21/2025 (PEE2025331000108).</funding_grant_id><funding_grant_id>404172/2023-7</funding_grant_id><funding_grant_id>401355/2025-0</funding_grant_id><funding_grant_id>Chamada Pública FAPEG N° 05/2025 (PVE2025041000055)</funding_grant_id><funding_grant_id>Chamada Pública FAPEG N° 21/2025 (PEE2025331000083)</funding_grant_id><funding_grant_id>405655/2023-1</funding_grant_id><funding_grant_id>316687/2023-5</funding_grant_id><funding_grant_id>Chamada Pública FAPEG/SES N° 18/2025 (ARB2025191000003)</funding_grant_id><pubmed_authors>Singh VP</pubmed_authors><pubmed_authors>Camara GA</pubmed_authors><pubmed_authors>Frizon TEA</pubmed_authors><pubmed_authors>Saba S</pubmed_authors><pubmed_authors>Botteselle GV</pubmed_authors><pubmed_authors>Stein AL</pubmed_authors><pubmed_authors>Rafique J</pubmed_authors><pubmed_authors>Schneider AR</pubmed_authors><pubmed_authors>Casagrande GA</pubmed_authors><pubmed_authors>Oliveira IME</pubmed_authors><pubmed_authors>Braga AL</pubmed_authors><pubmed_authors>Moraes CAO</pubmed_authors><pubmed_authors>Brito JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical Synthesis of 3-Selenyl-Chromones via Domino C(sp&lt;sup>2&lt;/sup>)-H Bond Selenylation/Annulation of Enaminones.</name><description>Herein, we disclose a highly efficient pathway toward 3-selenylated chromone derivatives via electrosynthesis domino C(sp&lt;sup>2&lt;/sup>)-H bond selenylation/cyclization/deamination of 2-hydroxyaryl enaminones with diselenides. This method showed mild conditions, easy operation, a wide substrate scope, and good functional group tolerance. Furthermore, this electrosynthesis strategy was amenable to scaling up the reaction. Additionally, the preliminary experiments revealed that this reaction probably proceeded via a cation pathway instead of a radical pathway.</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-09T03:18:44.832Z</modification><creation>2026-06-09T03:11:47.054Z</creation></dates><accession>S-EPMC12844472</accession><cross_references><pubmed>41599438</pubmed><doi>10.3390/molecules31020391</doi></cross_references></HashMap>