<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(6)</volume><submitter>He Y</submitter><pubmed_abstract>A metal-free, mild and efficient protocol for the construction of aroylated N-heterocycles &lt;i>via&lt;/i> radical cascade aroylation of phenyl or vinyl isocyanides with aromatic aldehydes has been developed. Both phenanthridine and isoquinoline derivatives are delivered quickly in moderate to good yields with high regioselectivity.</pubmed_abstract><journal>RSC advances</journal><pagination>3036-3040</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9077706</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Metal-free oxidative isocyanides insertion with aromatic aldehydes to aroylated N-heterocycles.</pubmed_title><pmcid>PMC9077706</pmcid><pubmed_authors>Gan C</pubmed_authors><pubmed_authors>Huang C</pubmed_authors><pubmed_authors>Xiao JA</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Pang J</pubmed_authors><pubmed_authors>Wang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metal-free oxidative isocyanides insertion with aromatic aldehydes to aroylated N-heterocycles.</name><description>A metal-free, mild and efficient protocol for the construction of aroylated N-heterocycles &lt;i>via&lt;/i> radical cascade aroylation of phenyl or vinyl isocyanides with aromatic aldehydes has been developed. Both phenanthridine and isoquinoline derivatives are delivered quickly in moderate to good yields with high regioselectivity.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2025-04-21T23:18:47Z</modification><creation>2025-02-19T03:24:57.618Z</creation></dates><accession>S-EPMC9077706</accession><cross_references><pubmed>35541179</pubmed><doi>10.1039/c7ra12755c</doi></cross_references></HashMap>