<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Qi C</submitter><funding>Nantong University</funding><funding>Science and Technology Project of Nantong City</funding><pagination>23147-23151</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11262084</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(32)</volume><pubmed_abstract>Zn(OTf)&lt;sub>2&lt;/sub>-catalyzed intra- and intermolecular selenofunctionalization of alkenes was achieved with electrophilic &lt;i>N&lt;/i>-phenylselenophthalimide. This method provides straightforward and efficient access to various seleno-substituted heterocycles and vicinal Se heteroatom-disubstituted molecules under mild conditions. This reaction is compatible with various substrates/functional groups, and preliminary studies on the reaction mechanistic were also conducted.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Zn(OTf)&lt;sub>2&lt;/sub>-catalyzed intra- and intermolecular selenofunctionalization of alkenes under mild conditions.</pubmed_title><pmcid>PMC11262084</pmcid><funding_grant_id>JC22022097</funding_grant_id><funding_grant_id>JC2023035</funding_grant_id><funding_grant_id>KFJN2365</funding_grant_id><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>Lu Z</pubmed_authors><pubmed_authors>Bao X</pubmed_authors><pubmed_authors>Xiong B</pubmed_authors><pubmed_authors>Qi C</pubmed_authors><pubmed_authors>Liu GQ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Zn(OTf)&lt;sub>2&lt;/sub>-catalyzed intra- and intermolecular selenofunctionalization of alkenes under mild conditions.</name><description>Zn(OTf)&lt;sub>2&lt;/sub>-catalyzed intra- and intermolecular selenofunctionalization of alkenes was achieved with electrophilic &lt;i>N&lt;/i>-phenylselenophthalimide. This method provides straightforward and efficient access to various seleno-substituted heterocycles and vicinal Se heteroatom-disubstituted molecules under mild conditions. This reaction is compatible with various substrates/functional groups, and preliminary studies on the reaction mechanistic were also conducted.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-05-18T13:26:57.814Z</modification><creation>2025-05-18T13:26:57.814Z</creation></dates><accession>S-EPMC11262084</accession><cross_references><pubmed>39040696</pubmed><doi>10.1039/d4ra04266b</doi></cross_references></HashMap>