<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Li Q</submitter><pubmed_abstract>The construction of the biologically interesting chromone skeleton was realized by PhIO-mediated dehydrogenation of chromanones under mild conditions. Interestingly, this method also found application in the synthesis of the naturally occurring frutinone A.</pubmed_abstract><journal>Beilstein journal of organic chemistry</journal><pagination>2958-2965</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6941426</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Construction of trisubstituted chromone skeletons carrying electron-withdrawing groups via PhIO-mediated dehydrogenation and its application to the synthesis of frutinone A.</pubmed_title><pmcid>PMC6941426</pmcid><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Zhuang C</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Jia R</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Sun F</pubmed_authors><pubmed_authors>Du Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Construction of trisubstituted chromone skeletons carrying electron-withdrawing groups via PhIO-mediated dehydrogenation and its application to the synthesis of frutinone A.</name><description>The construction of the biologically interesting chromone skeleton was realized by PhIO-mediated dehydrogenation of chromanones under mild conditions. Interestingly, this method also found application in the synthesis of the naturally occurring frutinone A.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2021-02-21T07:35:01Z</modification><creation>2020-05-22T07:34:35Z</creation></dates><accession>S-EPMC6941426</accession><cross_references><pubmed>31921367</pubmed><doi>10.3762/bjoc.15.291</doi></cross_references></HashMap>