<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bychek R</submitter><funding>European Research Council</funding><funding>HORIZON EUROPE European Research Council</funding><pagination>e202205103</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9401599</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(29)</volume><pubmed_abstract>After more than 20 years of trials, a practical scalable approach to fluoro-substituted bicyclo[1.1.1]pentanes (F-BCPs) has been developed. The physicochemical properties of the F-BCPs have been studied, and the core was incorporated into the structure of the anti-inflammatory drug Flurbiprofen in place of the fluorophenyl ring.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>A Practical and Scalable Approach to Fluoro-Substituted Bicyclo[1.1.1]pentanes.</pubmed_title><pmcid>PMC9401599</pmcid><funding_grant_id>101000893</funding_grant_id><pubmed_authors>Mykhailiuk PK</pubmed_authors><pubmed_authors>Bychek R</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Practical and Scalable Approach to Fluoro-Substituted Bicyclo[1.1.1]pentanes.</name><description>After more than 20 years of trials, a practical scalable approach to fluoro-substituted bicyclo[1.1.1]pentanes (F-BCPs) has been developed. The physicochemical properties of the F-BCPs have been studied, and the core was incorporated into the structure of the anti-inflammatory drug Flurbiprofen in place of the fluorophenyl ring.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-06-01T01:32:28.548Z</modification><creation>2025-06-01T01:32:28.548Z</creation></dates><accession>S-EPMC9401599</accession><cross_references><pubmed>35638404</pubmed><doi>10.1002/anie.202205103</doi></cross_references></HashMap>