<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ripenko V</submitter><funding>European Research Council</funding><pagination>14061-14068</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8524415</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>86(20)</volume><pubmed_abstract>&lt;i>In flow&lt;/i> photochemical addition of propellane to diacetyl allowed construction of the bicyclo[1.1.1]pentane (BCP) core in a 1 kg scale within 1 day. Haloform reaction of the formed diketone in batch afforded bicyclo[1.1.1]pentane-1,3-dicarboxylic acid in a multigram amount. Representative gram scale transformations of the diacid were also performed to obtain various BCP-containing building blocks-alcohols, acids, amines, trifluoroborates, amino acids, &lt;i>etc&lt;/i>.-for medicinal chemistry.</pubmed_abstract><journal>The Journal of organic chemistry</journal><pubmed_title>Large-Scale Synthesis and Modifications of Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid (BCP).</pubmed_title><pmcid>PMC8524415</pmcid><funding_grant_id>101000893</funding_grant_id><funding_grant_id>101000893 - BENOVELTY</funding_grant_id><pubmed_authors>Klymov I</pubmed_authors><pubmed_authors>Mykhailiuk PK</pubmed_authors><pubmed_authors>Zhersh S</pubmed_authors><pubmed_authors>Ripenko V</pubmed_authors><pubmed_authors>Vysochyn D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Large-Scale Synthesis and Modifications of Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid (BCP).</name><description>&lt;i>In flow&lt;/i> photochemical addition of propellane to diacetyl allowed construction of the bicyclo[1.1.1]pentane (BCP) core in a 1 kg scale within 1 day. Haloform reaction of the formed diketone in batch afforded bicyclo[1.1.1]pentane-1,3-dicarboxylic acid in a multigram amount. Representative gram scale transformations of the diacid were also performed to obtain various BCP-containing building blocks-alcohols, acids, amines, trifluoroborates, amino acids, &lt;i>etc&lt;/i>.-for medicinal chemistry.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-21T14:52:24.829Z</modification><creation>2024-11-19T19:07:47.554Z</creation></dates><accession>S-EPMC8524415</accession><cross_references><pubmed>34166594</pubmed><doi>10.1021/acs.joc.1c00977</doi></cross_references></HashMap>