<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lai YL</submitter><funding>Science and Technology Planning Project of Guangdong Province</funding><funding>Department of Education of Guangdong Province</funding><funding>Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology</funding><funding>Natural Science Foundation of Guangdong Province</funding><funding>National Natural Science Foundation of China</funding><pagination>28447-28451</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9037987</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(46)</volume><pubmed_abstract>An efficient and straightforward palladium-catalyzed three-component cascade bisthiolation of terminal alkynes and arylhydrazines with sodium thiosulfate (Na&lt;sub>2&lt;/sub>S&lt;sub>2&lt;/sub>O&lt;sub>3&lt;/sub>) as the sulfur source for the assembly of functionalized (&lt;i>Z&lt;/i>)-1,2-bis(arylthio)alkene derivatives is described. Using 0.5 mol% IPr-Pd-Im-Cl&lt;sub>2&lt;/sub> as the catalyst, a wide range of terminal alkynes and arylhydrazines are well tolerated, thus producing the desired products in good yields with good functional group tolerance and excellent regioselectivity. Moreover, this protocol could be readily scaled up, showing potential applications in organic synthesis and material science.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse (&lt;i>Z&lt;/i>)-1,2-bis(arylthio)alkene derivatives.</pubmed_title><pmcid>PMC9037987</pmcid><funding_grant_id>2018KQNCX236</funding_grant_id><funding_grant_id>2018B030308007</funding_grant_id><funding_grant_id>21971072</funding_grant_id><funding_grant_id>2019B030301003</funding_grant_id><pubmed_authors>Zhou LZ</pubmed_authors><pubmed_authors>Chen ZS</pubmed_authors><pubmed_authors>Du YL</pubmed_authors><pubmed_authors>He D</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Lai YL</pubmed_authors><pubmed_authors>Yan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse (&lt;i>Z&lt;/i>)-1,2-bis(arylthio)alkene derivatives.</name><description>An efficient and straightforward palladium-catalyzed three-component cascade bisthiolation of terminal alkynes and arylhydrazines with sodium thiosulfate (Na&lt;sub>2&lt;/sub>S&lt;sub>2&lt;/sub>O&lt;sub>3&lt;/sub>) as the sulfur source for the assembly of functionalized (&lt;i>Z&lt;/i>)-1,2-bis(arylthio)alkene derivatives is described. Using 0.5 mol% IPr-Pd-Im-Cl&lt;sub>2&lt;/sub> as the catalyst, a wide range of terminal alkynes and arylhydrazines are well tolerated, thus producing the desired products in good yields with good functional group tolerance and excellent regioselectivity. Moreover, this protocol could be readily scaled up, showing potential applications in organic synthesis and material science.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2025-04-05T11:07:20.363Z</modification><creation>2025-04-05T11:07:20.363Z</creation></dates><accession>S-EPMC9037987</accession><cross_references><pubmed>35478536</pubmed><doi>10.1039/d1ra05773a</doi></cross_references></HashMap>