<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(3)</volume><submitter>Abdelmoniem AM</submitter><funding>Alexander von Humboldt Foundation</funding><funding>Alexander von Humboldt-Stiftung</funding><pubmed_abstract>New Azacycles by One-Pot Three-Component Hantzsch-Like Synthesis of Tetra(hexa)azacyclopenta[a]anthracenes, Tetraazaindeno[5,4-b]fluorenes, and Oxatetraazacyclopenta[m]tetraphenes (H. Butenschön, I. A. Abdelhamid et al.) #OpenAccess Multicomponent reactions (MCRs) are envisaged as an entry point for the synthesis of heterocyclic compounds with interesting biological activities. An efficient approach to annelated tetra(hexa)azacyclopenta[a]anthracenes, tetraazaindeno[5,4-b]fluorenes, and oxatetraazacyclopenta[m]tetraphene was accomplished using a three-component reaction involving 7-amino-2-methyl-3-phenylpyrazolo[1,5-a]pyrimidin-5-one with aromatic aldehydes and the corresponding active 1,3-dicarbonyl compounds (namely, dimedone, 1,3-dimethylbarbituric acid, 1,3-indanedione, and 4-hydroxyc</pubmed_abstract><journal>ChemistryOpen</journal><pagination>e202300009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9975464</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>New Azacycles by One-Pot Three-Component Hantzsch-Like Synthesis of Tetra(hexa)azacyclopenta[a]anthracenes, Tetraazaindeno[5,4-b]fluorenes, and Oxatetraazacyclopenta[m]tetraphenes.</pubmed_title><pmcid>PMC9975464</pmcid><pubmed_authors>Butenschon H</pubmed_authors><pubmed_authors>Abdelhamid IA</pubmed_authors><pubmed_authors>Ghozlan SAS</pubmed_authors><pubmed_authors>Ramadan MA</pubmed_authors><pubmed_authors>Abdelmoniem AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>New Azacycles by One-Pot Three-Component Hantzsch-Like Synthesis of Tetra(hexa)azacyclopenta[a]anthracenes, Tetraazaindeno[5,4-b]fluorenes, and Oxatetraazacyclopenta[m]tetraphenes.</name><description>New Azacycles by One-Pot Three-Component Hantzsch-Like Synthesis of Tetra(hexa)azacyclopenta[a]anthracenes, Tetraazaindeno[5,4-b]fluorenes, and Oxatetraazacyclopenta[m]tetraphenes (H. Butenschön, I. A. Abdelhamid et al.) #OpenAccess Multicomponent reactions (MCRs) are envisaged as an entry point for the synthesis of heterocyclic compounds with interesting biological activities. An efficient approach to annelated tetra(hexa)azacyclopenta[a]anthracenes, tetraazaindeno[5,4-b]fluorenes, and oxatetraazacyclopenta[m]tetraphene was accomplished using a three-component reaction involving 7-amino-2-methyl-3-phenylpyrazolo[1,5-a]pyrimidin-5-one with aromatic aldehydes and the corresponding active 1,3-dicarbonyl compounds (namely, dimedone, 1,3-dimethylbarbituric acid, 1,3-indanedione, and 4-hydroxyc</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-03-17T15:46:09.45Z</modification><creation>2025-04-05T13:02:35.261Z</creation></dates><accession>S-EPMC9975464</accession><cross_references><pubmed>36855319</pubmed><doi>10.1002/open.202300009</doi></cross_references></HashMap>