{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["17(19)"],"submitter":["Wang C"],"funding":["China Scholarship Council"],"pubmed_abstract":["Treatment of N-methyl-S,S-diaryl sulfoximines with methyl trifluoromethanesulfonate provides bench-stable sulfoxinium salts in excellent yields. Applying them in Sonogashira-, Heck- and Suzuki-type cross-coupling reactions leads to the corresponding products by sequential C-S bond cleavage and C-C bond formation. Electronic factors induced by substituents on the S-aryl groups govern the coupling efficiency."],"journal":["Chemistry, an Asian journal"],"pagination":["e202200828"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9804342"],"repository":["biostudies-literature"],"pubmed_title":["The Preparation of Diaryl Sulfoxinium Triflates and Their Application in Palladium-Catalyzed Cross-Coupling Reactions."],"pmcid":["PMC9804342"],"pubmed_authors":["Wang C","Rissanen K","Truong KN","Kong D","Wang X","Bolm C"],"additional_accession":[]},"is_claimable":false,"name":"The Preparation of Diaryl Sulfoxinium Triflates and Their Application in Palladium-Catalyzed Cross-Coupling Reactions.","description":"Treatment of N-methyl-S,S-diaryl sulfoximines with methyl trifluoromethanesulfonate provides bench-stable sulfoxinium salts in excellent yields. Applying them in Sonogashira-, Heck- and Suzuki-type cross-coupling reactions leads to the corresponding products by sequential C-S bond cleavage and C-C bond formation. Electronic factors induced by substituents on the S-aryl groups govern the coupling efficiency.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Oct","modification":"2025-04-05T12:09:15.814Z","creation":"2025-04-05T12:09:15.814Z"},"accession":"S-EPMC9804342","cross_references":{"pubmed":["35947778"],"doi":["10.1002/asia.202200828"]}}