{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["12(38)"],"submitter":["Zhao Q"],"pubmed_abstract":["The palladium-catalyzed oxidative C-H olefinations of uridine, deoxyuridine, uridine monophosphate and uridine analogues are reported herein. This protocol provides an efficient, atom-economic and environmentally friendly approach to the synthesis of biologically important C5-alkene modified uracil/uridine-containing derivatives and pharmaceutical candidates."],"journal":["RSC advances"],"pagination":["24930-24934"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9434382"],"repository":["biostudies-literature"],"pubmed_title":["Palladium-catalyzed C-H olefination of uridine, deoxyuridine, uridine monophosphate and uridine analogues."],"pmcid":["PMC9434382"],"pubmed_authors":["Li W","Li Y","Zhao Q","Chen G","Xiao G","Zeng Y","Xie R"],"additional_accession":[]},"is_claimable":false,"name":"Palladium-catalyzed C-H olefination of uridine, deoxyuridine, uridine monophosphate and uridine analogues.","description":"The palladium-catalyzed oxidative C-H olefinations of uridine, deoxyuridine, uridine monophosphate and uridine analogues are reported herein. This protocol provides an efficient, atom-economic and environmentally friendly approach to the synthesis of biologically important C5-alkene modified uracil/uridine-containing derivatives and pharmaceutical candidates.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Aug","modification":"2025-04-19T10:00:04.475Z","creation":"2025-04-19T10:00:04.475Z"},"accession":"S-EPMC9434382","cross_references":{"pubmed":["36199883"],"doi":["10.1039/d2ra03681a"]}}