{"database":"biostudies-literature","file_versions":[],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":39,"searchCount":0},"additional":{"submitter":["Raushel J"],"funding":["NIGMS NIH HHS"],"pagination":["4952-5"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2982995"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["12(21)"],"pubmed_abstract":["An efficient room-temperature method for the synthesis of 1-sulfonyl-1,2,3-triazoles from in situ generated copper(I) acetylides and sulfonyl azides is described. The copper(I) thiophene-2-carboxylate (CuTC) catalyst produces the title compounds under both nonbasic anhydrous and aqueous conditions in good yields."],"journal":["Organic letters"],"pubmed_title":["Efficient synthesis of 1-sulfonyl-1,2,3-triazoles."],"pmcid":["PMC2982995"],"funding_grant_id":["GM087620","R01 GM087620"],"pubmed_authors":["Raushel J","Fokin VV"],"view_count":["39"],"additional_accession":[]},"is_claimable":false,"name":"Efficient synthesis of 1-sulfonyl-1,2,3-triazoles.","description":"An efficient room-temperature method for the synthesis of 1-sulfonyl-1,2,3-triazoles from in situ generated copper(I) acetylides and sulfonyl azides is described. The copper(I) thiophene-2-carboxylate (CuTC) catalyst produces the title compounds under both nonbasic anhydrous and aqueous conditions in good yields.","dates":{"release":"2010-01-01T00:00:00Z","publication":"2010 Nov","modification":"2024-11-14T13:46:49.981Z","creation":"2019-03-27T00:36:40Z"},"accession":"S-EPMC2982995","cross_references":{"pubmed":["20931987"],"doi":["10.1021/ol102087r"]}}