{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["8(6)"],"submitter":["He Y"],"pubmed_abstract":["A metal-free, mild and efficient protocol for the construction of aroylated N-heterocycles <i>via</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."],"journal":["RSC advances"],"pagination":["3036-3040"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9077706"],"repository":["biostudies-literature"],"pubmed_title":["Metal-free oxidative isocyanides insertion with aromatic aldehydes to aroylated N-heterocycles."],"pmcid":["PMC9077706"],"pubmed_authors":["Gan C","Huang C","Xiao JA","He Y","Huang Y","Pang J","Wang X"],"additional_accession":[]},"is_claimable":false,"name":"Metal-free oxidative isocyanides insertion with aromatic aldehydes to aroylated N-heterocycles.","description":"A metal-free, mild and efficient protocol for the construction of aroylated N-heterocycles <i>via</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.","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Jan","modification":"2025-04-21T23:18:47Z","creation":"2025-02-19T03:24:57.618Z"},"accession":"S-EPMC9077706","cross_references":{"pubmed":["35541179"],"doi":["10.1039/c7ra12755c"]}}