{"doi":"10.1002/jccs.201300358","title":"One‐pot Synthesis of Octahydroqinazolinones Derivatives Catalyzed by [C<sub>4</sub>(mim)<sub>2</sub>](FeCl<sub>4</sub>)<sub>2</sub> under Solvent Free Conditions","abstract":"<jats:title>Abstract</jats:title><jats:p>In this investigation, a practical green chemistry procedure for synthesis of octahydroqinazolinones and thiones derivatives via condensation of aldehyde, 1,3‐cyclohexanedione/dimedone and urea or thiourea catalyzed by magnetic room temperature dicationic liquid under solvent free conditions is described. The catalyst was studied by UV spectroscopy, vibrating sample magnetometer, and thermogravimetric analysis. This methodology is of interest due to several advantages such as environmental benign, easy experimental procedure, good yield and reusable catalyst.</jats:p>","journal":"Journal of the Chinese Chemical Society","year":2014,"id":602006,"datarank":0.32958368660043297,"base_score":2.1972245773362196,"endowment":2.1972245773362196,"self_citation_contribution":0.32958368660043297,"citation_network_contribution":0.0,"self_endowment_contribution":0.32958368660043297,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":8,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1543767,"name":"Soghra Soleimani","orcid":null,"position":1,"is_corresponding":false},{"id":1543765,"name":"Bijan Mombani Godajdar","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"One‐pot Synthesis of Octahydroqinazolinones Derivatives Catalyzed by [C<sub>4</sub>(mim)<sub>2</sub>](FeCl<sub>4</sub>)<sub>2</sub> under Solvent Free Conditions","abstract":"<jats:title>Abstract</jats:title><jats:p>In this investigation, a practical green chemistry procedure for synthesis of octahydroqinazolinones and thiones derivatives via condensation of aldehyde, 1,3‐cyclohexanedione/dimedone and urea or thiourea catalyzed by magnetic room temperature dicationic liquid under solvent free conditions is described. The catalyst was studied by UV spectroscopy, vibrating sample magnetometer, and thermogravimetric analysis. This methodology is of interest due to several advantages such as environmental benign, easy experimental procedure, good yield and reusable catalyst.</jats:p>","is_dataset_classified":null,"base_score":2.0794415416798357,"endowment":2.0794415416798357,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"21097893","pmcid":null,"openalex_id":"https://openalex.org/W2089202818","authors":[],"funders":[],"total_grants":0,"fwci":0.6411,"citation_percentile":0.6865373,"influential_citations":0,"citation_trend":[{"year":2014,"count":2},{"year":2015,"count":1},{"year":2017,"count":1},{"year":2018,"count":2},{"year":2026,"count":1}],"oa_status":"closed","license":"http://onlinelibrary.wiley.com/termsAndConditions#vor","oa_locations":[{"url":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjccs.201300358","host_type":"publisher"},{"url":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/jccs.201300358","host_type":"publisher"},{"url":"https://doi.org/10.1002/jccs.201300358","host_type":"journal"}],"fields_of_study":["Multicomponent Synthesis of Heterocycles","Synthesis and biological activity","Chemical Synthesis and Reactions"],"mesh_terms":[],"keywords":["Dimedone","Chemistry","Thiourea","Catalysis","Aldehyde","Thermogravimetric analysis","Condensation","Yield (engineering)","Green chemistry","Condensation reaction","Urea","Solvent","Organic chemistry","Nuclear chemistry","Reaction mechanism"],"sdg_mappings":[{"sdg_number":0,"sdg_label":"Life in Land"}],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-07-29T18:00:34.261936Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}