<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(22)</volume><submitter>Szafraniec A</submitter><pubmed_abstract>This paper presents the synthesis of a coumarin derivative of resorcin[4]arene (1) using a cascade thermolysis/Michael reaction. The influence of the hydrogen bonding system on the conformational rigidity and cyclochirality of the coumarin derivative of resorcin[4]arene was discussed; these properties depended on the proton-donor-acceptor properties of the solvent. Significant differences, which depended on the environment, in the coumarin derivative of resorcin[4]arene fluorescence were observed and discussed.</pubmed_abstract><journal>RSC advances</journal><pagination>12747-12753</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9051107</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis of a coumarin derivative of resorcin[4]arene with solvent-controlled chirality.</pubmed_title><pmcid>PMC9051107</pmcid><pubmed_authors>Iwanek W</pubmed_authors><pubmed_authors>Szafraniec A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis of a coumarin derivative of resorcin[4]arene with solvent-controlled chirality.</name><description>This paper presents the synthesis of a coumarin derivative of resorcin[4]arene (1) using a cascade thermolysis/Michael reaction. The influence of the hydrogen bonding system on the conformational rigidity and cyclochirality of the coumarin derivative of resorcin[4]arene was discussed; these properties depended on the proton-donor-acceptor properties of the solvent. Significant differences, which depended on the environment, in the coumarin derivative of resorcin[4]arene fluorescence were observed and discussed.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Mar</publication><modification>2025-04-19T00:40:36.827Z</modification><creation>2025-04-07T11:41:48.48Z</creation></dates><accession>S-EPMC9051107</accession><cross_references><pubmed>35492126</pubmed><doi>10.1039/d0ra00368a</doi></cross_references></HashMap>