{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["24(3)"],"submitter":["Long Y"],"pubmed_abstract":["A simple protocol of iron(III)-catalyzed halogenation of 8-amidoquinolines in water under mild conditions was developed, affording the 5-halogenlated products in good to excellent yields up to 98%. The reaction mechanism most likely involves a single-electron transfer (SET) process."],"journal":["Molecules (Basel, Switzerland)"],"pagination":["E535"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6384643"],"repository":["biostudies-literature"],"pubmed_title":["Iron(III)-Catalyzed Highly Regioselective Halogenation of 8-Amidoquinolines in Water."],"pmcid":["PMC6384643"],"pubmed_authors":["Long Y","Pan L","Zhou X"],"additional_accession":[]},"is_claimable":false,"name":"Iron(III)-Catalyzed Highly Regioselective Halogenation of 8-Amidoquinolines in Water.","description":"A simple protocol of iron(III)-catalyzed halogenation of 8-amidoquinolines in water under mild conditions was developed, affording the 5-halogenlated products in good to excellent yields up to 98%. The reaction mechanism most likely involves a single-electron transfer (SET) process.","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Feb","modification":"2024-11-15T22:23:09.387Z","creation":"2019-08-04T07:36:56Z"},"accession":"S-EPMC6384643","cross_references":{"pubmed":["30717184"],"doi":["10.3390/molecules24030535"]}}