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