<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(6)</volume><submitter>Yao G</submitter><pubmed_abstract>DMSO was found to activate arylisothiocyanates for self-nucleophilic addition. A subsequent intramolecular C-H sulfurization catalyzed by PdBr&lt;sub>2&lt;/sub> enables access to a wide range of 2-aminobenzothiazole derivatives in moderate to good yields. This is the first example of a DMSO-mediated Pd-catalyzed synthesis of 2-aminobenzothiazoles through cyclization/C-H sulfurization of two isothiocyanates.</pubmed_abstract><journal>RSC advances</journal><pagination>3403-3406</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9060301</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>DMSO-mediated palladium-catalyzed cyclization of two isothiocyanates &lt;i>via&lt;/i> C-H sulfurization: a new route to 2-aminobenzothiazoles.</pubmed_title><pmcid>PMC9060301</pmcid><pubmed_authors>Wang BF</pubmed_authors><pubmed_authors>Zhang ZX</pubmed_authors><pubmed_authors>Yao G</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Xu HH</pubmed_authors><pubmed_authors>Tang RY</pubmed_authors></additional><is_claimable>false</is_claimable><name>DMSO-mediated palladium-catalyzed cyclization of two isothiocyanates &lt;i>via&lt;/i> C-H sulfurization: a new route to 2-aminobenzothiazoles.</name><description>DMSO was found to activate arylisothiocyanates for self-nucleophilic addition. A subsequent intramolecular C-H sulfurization catalyzed by PdBr&lt;sub>2&lt;/sub> enables access to a wide range of 2-aminobenzothiazole derivatives in moderate to good yields. This is the first example of a DMSO-mediated Pd-catalyzed synthesis of 2-aminobenzothiazoles through cyclization/C-H sulfurization of two isothiocyanates.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-04-04T20:21:53.563Z</modification><creation>2025-04-04T20:21:53.563Z</creation></dates><accession>S-EPMC9060301</accession><cross_references><pubmed>35518944</pubmed><doi>10.1039/c8ra09784d</doi></cross_references></HashMap>