{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["14(14)"],"submitter":["Yang Y"],"pubmed_abstract":["We disclosed herein a straightforward strategy for the synthesis of unprecedented <i>N</i>-((trifluoromethyl)thio), <i>N</i>-(trifluoromethyl) amines using a combination of isothiocyanates with a fluoride source and an electrophilic trifluoromethylthiolation reagent. More interestingly, the scalability of the methodology has been demonstrated and the stability of the new motif has been studied."],"journal":["Chemical science"],"pagination":["3893-3898"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10074438"],"repository":["biostudies-literature"],"pubmed_title":["Novel N(SCF<sub>3</sub>)(CF<sub>3</sub>)-amines: synthesis, scalability and stability."],"pmcid":["PMC10074438"],"pubmed_authors":["Yang Y","Saffon-Merceron N","Vantourout JC","Tlili A"],"additional_accession":[]},"is_claimable":false,"name":"Novel N(SCF<sub>3</sub>)(CF<sub>3</sub>)-amines: synthesis, scalability and stability.","description":"We disclosed herein a straightforward strategy for the synthesis of unprecedented <i>N</i>-((trifluoromethyl)thio), <i>N</i>-(trifluoromethyl) amines using a combination of isothiocyanates with a fluoride source and an electrophilic trifluoromethylthiolation reagent. More interestingly, the scalability of the methodology has been demonstrated and the stability of the new motif has been studied.","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Apr","modification":"2025-04-05T12:18:30.685Z","creation":"2025-04-05T12:18:30.685Z"},"accession":"S-EPMC10074438","cross_references":{"pubmed":["37035709"],"doi":["10.1039/d2sc06542h"]}}