{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Cheng K"],"funding":["NIBIB NIH HHS","National Institute of Biomedical Imaging and Bioengineering"],"pagination":["3419-3423"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11099534"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["26(16)"],"pubmed_abstract":["We present a photo- and Cu-mediated <sup>11</sup>C cyanation of bench-stable (hetero)aryl thianthrenium salts via an aryl radical addition pathway. The thianthrenium substrates can be readily accessed via C-H functionalization, and the radiocyanation protocol proceeds under mild conditions (<50 °C, 5 min) and can be automated using open-source, readily accessible augmentations to existing radiochemistry equipment."],"journal":["Organic letters"],"pubmed_title":["Photo- and Cu-Mediated <sup>11</sup>C Cyanation of (Hetero)Aryl Thianthrenium Salts."],"pmcid":["PMC11099534"],"funding_grant_id":["K99 EB031564","R01 EB021155","R01EB021155","K99EB031564"],"pubmed_authors":["Scott PJH","Shao X","Wright JS","Sanford MS","Cheng K","Bowden GD","Webb EW"],"additional_accession":[]},"is_claimable":false,"name":"Photo- and Cu-Mediated <sup>11</sup>C Cyanation of (Hetero)Aryl Thianthrenium Salts.","description":"We present a photo- and Cu-mediated <sup>11</sup>C cyanation of bench-stable (hetero)aryl thianthrenium salts via an aryl radical addition pathway. The thianthrenium substrates can be readily accessed via C-H functionalization, and the radiocyanation protocol proceeds under mild conditions (<50 °C, 5 min) and can be automated using open-source, readily accessible augmentations to existing radiochemistry equipment.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Apr","modification":"2025-07-01T03:05:47.039Z","creation":"2025-07-01T03:05:47.039Z"},"accession":"S-EPMC11099534","cross_references":{"pubmed":["38630573"],"doi":["10.1021/acs.orglett.4c00929"]}}