<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(32)</volume><submitter>Zhang T</submitter><pubmed_abstract>Synthetic methods for the preparation of thioketals featuring CF&lt;sub>3&lt;/sub> groups are rare. Here, we have developed a copper-catalyzed thioketalization of enones bearing CF&lt;sub>3&lt;/sub> groups and various mercaptans. 24 thioketal molecules have been obtained with moderate to excellent yield. Meanwhile, a preparative scale experiment has been performed giving over 95% yield. This work allows the straightforward formation of thioketals containing CF&lt;sub>3&lt;/sub> groups and unsaturated double bonds.</pubmed_abstract><journal>RSC advances</journal><pagination>19832-19835</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9033665</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups.</pubmed_title><pmcid>PMC9033665</pmcid><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Gao Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups.</name><description>Synthetic methods for the preparation of thioketals featuring CF&lt;sub>3&lt;/sub> groups are rare. Here, we have developed a copper-catalyzed thioketalization of enones bearing CF&lt;sub>3&lt;/sub> groups and various mercaptans. 24 thioketal molecules have been obtained with moderate to excellent yield. Meanwhile, a preparative scale experiment has been performed giving over 95% yield. This work allows the straightforward formation of thioketals containing CF&lt;sub>3&lt;/sub> groups and unsaturated double bonds.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2025-04-25T22:56:43.973Z</modification><creation>2025-04-06T09:14:16.664Z</creation></dates><accession>S-EPMC9033665</accession><cross_references><pubmed>35479255</pubmed><doi>10.1039/d1ra03222d</doi></cross_references></HashMap>