{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["10(62)"],"submitter":["Kuboki Y"],"pubmed_abstract":["Herein, we report a ring-opening 1,3-arylboration of aryl cyclopropanes using BCl<sub>3</sub> in the presence of arene nucleophiles. Formal 1,3-oxy arylation and 1,3-amino arylation of the arylcyclopropane <i>via</i> one-pot derivatization of the installed boron group were also achieved."],"journal":["RSC advances"],"pagination":["37797-37799"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9057229"],"repository":["biostudies-literature"],"pubmed_title":["Ring-opening 1,3-arylboration of arylcyclopropanes mediated by BCl<sub>3</sub>."],"pmcid":["PMC9057229"],"pubmed_authors":["Kuboki Y","Murai K","Arisawa M"],"additional_accession":[]},"is_claimable":false,"name":"Ring-opening 1,3-arylboration of arylcyclopropanes mediated by BCl<sub>3</sub>.","description":"Herein, we report a ring-opening 1,3-arylboration of aryl cyclopropanes using BCl<sub>3</sub> in the presence of arene nucleophiles. Formal 1,3-oxy arylation and 1,3-amino arylation of the arylcyclopropane <i>via</i> one-pot derivatization of the installed boron group were also achieved.","dates":{"release":"2020-01-01T00:00:00Z","publication":"2020 Oct","modification":"2025-04-04T12:56:22.622Z","creation":"2025-04-04T12:56:22.622Z"},"accession":"S-EPMC9057229","cross_references":{"pubmed":["35515187"],"doi":["10.1039/d0ra08151e"]}}