<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>52(48)</volume><submitter>Xu X</submitter><funding>NIGMS NIH HHS</funding><journal>Angewandte Chemie (International ed. in English)</journal><pagination>12664-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3858852</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Highly enantioselective dearomatizing formal [3+3] cycloaddition reactions of N-acyliminopyridinium ylides with electrophilic enol carbene intermediates.</pubmed_title><pmcid>PMC3858852</pmcid><funding_grant_id>GM 46503</funding_grant_id><funding_grant_id>R37 GM046503</funding_grant_id><funding_grant_id>R01 GM046503</funding_grant_id><pubmed_authors>Doyle MP</pubmed_authors><pubmed_authors>Zavalij PY</pubmed_authors><pubmed_authors>Xu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Highly enantioselective dearomatizing formal [3+3] cycloaddition reactions of N-acyliminopyridinium ylides with electrophilic enol carbene intermediates.</name><description/><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Nov</publication><modification>2025-04-04T20:51:52.65Z</modification><creation>2025-04-04T20:51:52.65Z</creation></dates><accession>S-EPMC3858852</accession><cross_references><pubmed>24123489</pubmed><doi>10.1002/anie.201305539</doi></cross_references></HashMap>