<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Piedra HF</submitter><funding>Fundación para el Fomento en Asturias de la Investigación Científica Aplicada y la Tecnología</funding><funding>Ministerio de Ciencia, Innovación y Universidades</funding><funding>Universidad de Oviedo</funding><pubmed_abstract>The first visible-light-induced protocol for the general preparation of alkenyl thiocyanates from alkenyl bromides is presented. The reaction is simple, proceeds under very mild conditions and demonstrates broad functional group tolerance. Additionally, a flow protocol was developed to enable efficient scale-up of alkenyl thiocyanate synthesis, further enhancing the practicality and value of the method. Importantly, these alkenyl thiocyanates serve as valuable building blocks for the construction of diverse families of sulfur-containing molecules through trifluoromethylations, cycloadditions, oxidations, and C-S or P-S bond forming reactions.</pubmed_abstract><journal>Chemical science</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11523809</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Visible-light-driven synthesis of alkenyl thiocyanates: novel building blocks for assembly of diverse sulfur-containing molecules.</pubmed_title><pmcid>PMC11523809</pmcid><funding_grant_id>BP21/050</funding_grant_id><funding_grant_id>MCINN-23-PID2022-140635NB-I00</funding_grant_id><funding_grant_id>MCINN-24-RYC2022-035485-I</funding_grant_id><funding_grant_id>PAPI-23-GR-COM-04</funding_grant_id><pubmed_authors>Plaza M</pubmed_authors><pubmed_authors>Piedra HF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Visible-light-driven synthesis of alkenyl thiocyanates: novel building blocks for assembly of diverse sulfur-containing molecules.</name><description>The first visible-light-induced protocol for the general preparation of alkenyl thiocyanates from alkenyl bromides is presented. The reaction is simple, proceeds under very mild conditions and demonstrates broad functional group tolerance. Additionally, a flow protocol was developed to enable efficient scale-up of alkenyl thiocyanate synthesis, further enhancing the practicality and value of the method. Importantly, these alkenyl thiocyanates serve as valuable building blocks for the construction of diverse families of sulfur-containing molecules through trifluoromethylations, cycloadditions, oxidations, and C-S or P-S bond forming reactions.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-04T20:38:43.25Z</modification><creation>2025-04-04T20:38:43.25Z</creation></dates><accession>S-EPMC11523809</accession><cross_references><pubmed>39483256</pubmed><doi>10.1039/d4sc06550f</doi></cross_references></HashMap>