<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Orrego-Hernandez J</submitter><funding>Facultad de Ciencias, Universidad de los Andes</funding><funding>Departamento Administrativo de Ciencia, Tecnología e Innovación</funding><pagination>27318-27323</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9070601</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(47)</volume><pubmed_abstract>A green process to access pyrazolo-fused 4-azafluorenones (indeno[1,2-&lt;i>b&lt;/i>]pyrazolo[4,3-&lt;i>e&lt;/i>]pyridines, IPP) 4a-x&lt;i>via&lt;/i> the three-component reaction between indan-1,3-dione (1), benzaldehydes 2 and 5-amino-1-arylpyrazoles 3 is described. These compounds were successfully used as precursors of the novel dicyanovinylidene derivatives 7a-d containing different acceptor (A) or donor (D) aryl groups at position 4 of its fused system. The structures of products obtained (4a-x and 7a-d) were determined based on NMR experiments, HRMS analysis, and X-ray diffraction studies for 7b. The photophysical and computational studies of 7a-d showed that these products are modulable ICT fluorophores, even some preliminary tests revealed that these compounds could be used as fluorescent chemodosim</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Pyrazolo-fused 4-azafluorenones as key reagents for the synthesis of fluorescent dicyanovinylidene-substituted derivatives.</pubmed_title><pmcid>PMC9070601</pmcid><funding_grant_id>Project Code 120465843502</funding_grant_id><pubmed_authors>Orrego-Hernandez J</pubmed_authors><pubmed_authors>Lizarazo C</pubmed_authors><pubmed_authors>Portilla J</pubmed_authors><pubmed_authors>Cobo J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pyrazolo-fused 4-azafluorenones as key reagents for the synthesis of fluorescent dicyanovinylidene-substituted derivatives.</name><description>A green process to access pyrazolo-fused 4-azafluorenones (indeno[1,2-&lt;i>b&lt;/i>]pyrazolo[4,3-&lt;i>e&lt;/i>]pyridines, IPP) 4a-x&lt;i>via&lt;/i> the three-component reaction between indan-1,3-dione (1), benzaldehydes 2 and 5-amino-1-arylpyrazoles 3 is described. These compounds were successfully used as precursors of the novel dicyanovinylidene derivatives 7a-d containing different acceptor (A) or donor (D) aryl groups at position 4 of its fused system. The structures of products obtained (4a-x and 7a-d) were determined based on NMR experiments, HRMS analysis, and X-ray diffraction studies for 7b. The photophysical and computational studies of 7a-d showed that these products are modulable ICT fluorophores, even some preliminary tests revealed that these compounds could be used as fluorescent chemodosim</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Aug</publication><modification>2025-04-04T09:10:17.774Z</modification><creation>2025-04-04T09:10:17.774Z</creation></dates><accession>S-EPMC9070601</accession><cross_references><pubmed>35529179</pubmed><doi>10.1039/c9ra04682h</doi></cross_references></HashMap>