<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guan W</submitter><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pagination>3231-3237</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6112771</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50(16)</volume><pubmed_abstract>Cross-couplings of benzylic pyridinium salts and vinylboronic acids or esters have been developed. Via these benzylic pyridinium intermediates, benzylic amines can be engaged in these cross-couplings via C-N bond functionalization. This method boasts mild reaction conditions and excellent tolerance for heteroaryl substituents and a range of functional groups.</pubmed_abstract><journal>Synthesis</journal><pubmed_title>Vinylation of Benzylic Amines via C-N Bond Functionalization of Benzylic Pyridinium Salts.</pubmed_title><pmcid>PMC6112771</pmcid><funding_grant_id>P30 GM110758</funding_grant_id><funding_grant_id>P20 GM104316</funding_grant_id><funding_grant_id>R01 GM111820</funding_grant_id><funding_grant_id>P20 GM103541</funding_grant_id><funding_grant_id>S10 OD016267</funding_grant_id><pubmed_authors>Liao J</pubmed_authors><pubmed_authors>Guan W</pubmed_authors><pubmed_authors>Watson MP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vinylation of Benzylic Amines via C-N Bond Functionalization of Benzylic Pyridinium Salts.</name><description>Cross-couplings of benzylic pyridinium salts and vinylboronic acids or esters have been developed. Via these benzylic pyridinium intermediates, benzylic amines can be engaged in these cross-couplings via C-N bond functionalization. This method boasts mild reaction conditions and excellent tolerance for heteroaryl substituents and a range of functional groups.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2024-02-16T02:56:20.341Z</modification><creation>2019-08-07T07:02:26Z</creation></dates><accession>S-EPMC6112771</accession><cross_references><pubmed>30174353</pubmed><doi>10.1055/s-0037-1610084</doi></cross_references></HashMap>