{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Chen D"],"funding":["National Natural Science Foundation of China"],"pagination":["1601-1606"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5361865"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["8(2)"],"pubmed_abstract":["An environmentally benign method for C-H/O-H difunctionalization of phenols with sulfoxides under mild conditions has been developed. The reaction process is mediated by an electrophilic aromatic substitution and subsequent selective aryl or alkyl migration, involving C-S and C-O bond formations with broad substrate scope."],"journal":["Chemical science"],"pubmed_title":["Metal-free O-H/C-H difunctionalization of phenols by <i>o</i>-hydroxyarylsulfonium salts in water."],"pmcid":["PMC5361865"],"funding_grant_id":["21502094"],"pubmed_authors":["Cai XM","Huang S","Yang Y","Wang F","Chen D","Feng Q"],"additional_accession":[]},"is_claimable":false,"name":"Metal-free O-H/C-H difunctionalization of phenols by <i>o</i>-hydroxyarylsulfonium salts in water.","description":"An environmentally benign method for C-H/O-H difunctionalization of phenols with sulfoxides under mild conditions has been developed. The reaction process is mediated by an electrophilic aromatic substitution and subsequent selective aryl or alkyl migration, involving C-S and C-O bond formations with broad substrate scope.","dates":{"release":"2017-01-01T00:00:00Z","publication":"2017 Feb","modification":"2025-04-05T15:14:06.956Z","creation":"2019-03-27T02:39:16Z"},"accession":"S-EPMC5361865","cross_references":{"pubmed":["28451289"],"doi":["10.1039/c6sc04504a"]}}