<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>129(15)</volume><submitter>Mattson AE</submitter><funding>NIGMS NIH HHS</funding><journal>Journal of the American Chemical Society</journal><pagination>4508-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2586065</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Nucleophilic acylation of o-quinone methides: an umpolung strategy for the synthesis of alpha-aryl ketones and benzofurans.</pubmed_title><pmcid>PMC2586065</pmcid><funding_grant_id>R01 GM 73072</funding_grant_id><funding_grant_id>R01 GM073072-02</funding_grant_id><funding_grant_id>R01 GM073072</funding_grant_id><pubmed_authors>Scheidt KA</pubmed_authors><pubmed_authors>Mattson AE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nucleophilic acylation of o-quinone methides: an umpolung strategy for the synthesis of alpha-aryl ketones and benzofurans.</name><description/><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Apr</publication><modification>2025-04-05T11:52:00.748Z</modification><creation>2025-04-05T11:52:00.748Z</creation></dates><accession>S-EPMC2586065</accession><cross_references><pubmed>17378561</pubmed><doi>10.1021/ja068189n</doi></cross_references></HashMap>