<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dong Y</submitter><funding>Chengdu Normal University</funding><pagination>3783-3787</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8979275</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(6)</volume><pubmed_abstract>An atom-economical approach for the synthesis of arylquinones was achieved successfully &lt;i>via&lt;/i> direct oxidative C-C dehydrogenative coupling reaction of quinones/hydroquinones with electron-rich arenes using an inexpensive Fe-I&lt;sub>2&lt;/sub>-(NH&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>S&lt;sub>2&lt;/sub>O&lt;sub>8&lt;/sub> system. The efficiency of this catalytic approach was established with a broad scope of substrates involving quinones and hydroquinones to give high yields (60-89%) of several arylated quinones. The present protocol is simple, practical, and shows good functional group tolerance.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Iron catalyzed C-C dehydrogenative coupling reaction: synthesis of arylquinones from quinones/hydroquinones.</pubmed_title><pmcid>PMC8979275</pmcid><funding_grant_id>2021CS21ZCY02</funding_grant_id><pubmed_authors>Dong Y</pubmed_authors><pubmed_authors>Shen A</pubmed_authors><pubmed_authors>Chang B</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Wang ZF</pubmed_authors><pubmed_authors>Shi ZC</pubmed_authors><pubmed_authors>He B</pubmed_authors><pubmed_authors>Xie C</pubmed_authors><pubmed_authors>Luo QQ</pubmed_authors><pubmed_authors>Yang F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Iron catalyzed C-C dehydrogenative coupling reaction: synthesis of arylquinones from quinones/hydroquinones.</name><description>An atom-economical approach for the synthesis of arylquinones was achieved successfully &lt;i>via&lt;/i> direct oxidative C-C dehydrogenative coupling reaction of quinones/hydroquinones with electron-rich arenes using an inexpensive Fe-I&lt;sub>2&lt;/sub>-(NH&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>S&lt;sub>2&lt;/sub>O&lt;sub>8&lt;/sub> system. The efficiency of this catalytic approach was established with a broad scope of substrates involving quinones and hydroquinones to give high yields (60-89%) of several arylated quinones. The present protocol is simple, practical, and shows good functional group tolerance.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-19T13:01:11.14Z</modification><creation>2025-04-19T13:01:11.14Z</creation></dates><accession>S-EPMC8979275</accession><cross_references><pubmed>35425366</pubmed><doi>10.1039/d1ra08828a</doi></cross_references></HashMap>