{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Wang T"],"funding":["National Natural Science Foundation of China"],"pagination":["5738-5741"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9060798"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["9(10)"],"pubmed_abstract":["N-heterocyclic carbene-palladium(ii)-catalyzed cross-coupling of benzylammonium salts with arylboronic acids for the synthesis of diarylmethane derivatives <i>via</i> C-N bond activation has been developed. Notably, in the presence of the easily prepared and bench-stable Pd-PEPPSI precatalyst, the Csp<sup>3</sup>-N bond activation of the benzylammonium salt even proceeded smoothly in isopropanol at room temperature."],"journal":["RSC advances"],"pubmed_title":["Cross coupling of benzylammonium salts with boronic acids using a well-defined N-heterocyclic carbene-palladium(ii) precatalyst."],"pmcid":["PMC9060798"],"funding_grant_id":["U1504207","21572126"],"pubmed_authors":["Guo J","Liu L","Jia D","Guo H","Wang T","Wang X","Wang H"],"additional_accession":[]},"is_claimable":false,"name":"Cross coupling of benzylammonium salts with boronic acids using a well-defined N-heterocyclic carbene-palladium(ii) precatalyst.","description":"N-heterocyclic carbene-palladium(ii)-catalyzed cross-coupling of benzylammonium salts with arylboronic acids for the synthesis of diarylmethane derivatives <i>via</i> C-N bond activation has been developed. Notably, in the presence of the easily prepared and bench-stable Pd-PEPPSI precatalyst, the Csp<sup>3</sup>-N bond activation of the benzylammonium salt even proceeded smoothly in isopropanol at room temperature.","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Feb","modification":"2025-04-04T23:17:16.857Z","creation":"2025-04-04T23:17:16.857Z"},"accession":"S-EPMC9060798","cross_references":{"pubmed":["35515917"],"doi":["10.1039/c8ra10439e"]}}