<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2(4)</volume><submitter>Zhu M</submitter><pubmed_abstract>Here, we report a one-pot Stadler-Ziegler reaction toward the synthesis of 1-thioglycosides in good yield from commercially available anilines and (un)protected 1-glycosyl thiols. This simple and mild approach employs the photoredox catalyst [Ru(bpy)&lt;sub>3&lt;/sub>](PF&lt;sub>6&lt;/sub>)&lt;sub>2&lt;/sub> under visible light.</pubmed_abstract><journal>ACS organic &amp; inorganic Au</journal><pagination>351-358</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9955296</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Visible-Light-Mediated Stadler-Ziegler Arylation of Thiosugars with Anilines.</pubmed_title><pmcid>PMC9955296</pmcid><pubmed_authors>Zhu M</pubmed_authors><pubmed_authors>Ghouilem J</pubmed_authors><pubmed_authors>Messaoudi S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Visible-Light-Mediated Stadler-Ziegler Arylation of Thiosugars with Anilines.</name><description>Here, we report a one-pot Stadler-Ziegler reaction toward the synthesis of 1-thioglycosides in good yield from commercially available anilines and (un)protected 1-glycosyl thiols. This simple and mild approach employs the photoredox catalyst [Ru(bpy)&lt;sub>3&lt;/sub>](PF&lt;sub>6&lt;/sub>)&lt;sub>2&lt;/sub> under visible light.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-26T10:18:29.812Z</modification><creation>2025-04-06T13:17:03.776Z</creation></dates><accession>S-EPMC9955296</accession><cross_references><pubmed>36855591</pubmed><doi>10.1021/acsorginorgau.2c00006</doi></cross_references></HashMap>