<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Karmakar I</submitter><funding>Science and Engineering Research Board</funding><funding>National Chung-Hsing University</funding><funding>National Science and Technology Council</funding><funding>Ministry of Education, Taiwan</funding><pagination>12205-12215</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12400415</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>90(34)</volume><pubmed_abstract>We report a robust and eco-conscious electrosynthetic protocol for efficiently constructing structurally diverse and biologically relevant dibenzoselenophenes. This transformation proceeds &lt;i>via&lt;/i> electrochemical intramolecular C-H activation of bis(biaryl) diselenides, employing LiClO&lt;sub>4&lt;/sub> as a green electrolyte and tetrabutylammonium bromide as an additive, conducted in DMSO at 70 °C under a constant current of 10 mA using Pt/Pt electrodes. The newly developed method offers several notable advantages, including mild and energy-efficient conditions, transition-metal-free catalysis, short reaction times, high to excellent yields, broad substrate tolerance, scalability to gram-scale synthesis, operational simplicity, and environmental friendliness.</pubmed_abstract><journal>The Journal of organic chemistry</journal><pubmed_title>Site-Selective Electrochemical Intramolecular C(sp&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt;)-H Selenylation for Dibenzoselenophene Synthesis.</pubmed_title><pmcid>PMC12400415</pmcid><funding_grant_id>113-2113-M-005-014</funding_grant_id><pubmed_authors>Jian YX</pubmed_authors><pubmed_authors>Cheng WL</pubmed_authors><pubmed_authors>Karmakar I</pubmed_authors><pubmed_authors>Bai R</pubmed_authors><pubmed_authors>Chen YH</pubmed_authors><pubmed_authors>Lee CF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Site-Selective Electrochemical Intramolecular C(sp&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt;)-H Selenylation for Dibenzoselenophene Synthesis.</name><description>We report a robust and eco-conscious electrosynthetic protocol for efficiently constructing structurally diverse and biologically relevant dibenzoselenophenes. This transformation proceeds &lt;i>via&lt;/i> electrochemical intramolecular C-H activation of bis(biaryl) diselenides, employing LiClO&lt;sub>4&lt;/sub> as a green electrolyte and tetrabutylammonium bromide as an additive, conducted in DMSO at 70 °C under a constant current of 10 mA using Pt/Pt electrodes. The newly developed method offers several notable advantages, including mild and energy-efficient conditions, transition-metal-free catalysis, short reaction times, high to excellent yields, broad substrate tolerance, scalability to gram-scale synthesis, operational simplicity, and environmental friendliness.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-29T11:35:45.242Z</modification><creation>2026-04-08T04:26:09.349Z</creation></dates><accession>S-EPMC12400415</accession><cross_references><pubmed>40825176</pubmed><doi>10.1021/acs.joc.5c01600</doi></cross_references></HashMap>