<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Vemuri PY</submitter><funding>European Research Council</funding><funding>Deutsche Forschungsgemeinschaft</funding><pagination>1626-1630</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8902801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(8)</volume><pubmed_abstract>Oxidative clicklike reactions are useful for the late-stage functionalization of pharmaceuticals and organic materials. Hence, novel methodologies that enable such transformations are in high demand. Herein we describe a tellurium(II)-catalyzed cross-dehydrogenative phenothiazination (CDP) of aromatic amines. A key feature of this method is a cooperative effect between the phenotellurazine catalyst and the silver salt, which serves as a chemical oxidant for the reaction. This novel catalysis concept therefore enables a considerably broader scope compared with previous chemical oxidation methods.</pubmed_abstract><journal>Organic letters</journal><pubmed_title>Te(II)-Catalyzed Cross-Dehydrogenative Phenothiazination of Anilines.</pubmed_title><pmcid>PMC8902801</pmcid><funding_grant_id>SFB/TRR 88</funding_grant_id><funding_grant_id>716136</funding_grant_id><pubmed_authors>Vemuri PY</pubmed_authors><pubmed_authors>Cremer C</pubmed_authors><pubmed_authors>Patureau FW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Te(II)-Catalyzed Cross-Dehydrogenative Phenothiazination of Anilines.</name><description>Oxidative clicklike reactions are useful for the late-stage functionalization of pharmaceuticals and organic materials. Hence, novel methodologies that enable such transformations are in high demand. Herein we describe a tellurium(II)-catalyzed cross-dehydrogenative phenothiazination (CDP) of aromatic amines. A key feature of this method is a cooperative effect between the phenotellurazine catalyst and the silver salt, which serves as a chemical oxidant for the reaction. This novel catalysis concept therefore enables a considerably broader scope compared with previous chemical oxidation methods.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-26T04:37:08.982Z</modification><creation>2025-04-06T11:12:50.128Z</creation></dates><accession>S-EPMC8902801</accession><cross_references><pubmed>35192766</pubmed><doi>10.1021/acs.orglett.2c00125</doi></cross_references></HashMap>