{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T18:07:58Z","timestamp":1792174078572,"version":"4.4.0"},"reference-count":208,"publisher":"American Chemical Society (ACS)","issue":"42","license":[{"start":{"date-parts":[[2024,10,14]],"date-time":"2024-10-14T00:00:00Z","timestamp":1728864000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,10,22]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Heterocyclic compounds are of great interest in our daily lives. They are widely distributed in nature and are synthesized in laboratories. Heterocycles play an important role in the metabolism of all living cells, including vitamins and coenzyme precursors like thiamine and riboflavin. Furthermore, heterocyclic systems are essential building blocks for creating innovative materials with intriguing electrical, mechanical, and biological properties. Also, more than 85% of all biologically active chemical entities comprise a heterocycle. As a result, heterocycle synthesis piqued researchers\u2019 curiosity, and in recent decades, chemists have concentrated more on nitrogen-containing cyclic nuclei in structures. Quinoline and its derivatives exhibit several biological functions, including antimicrobial, anticancer, antimalarial, anti-inflammatory, antihypertensive, and antiasthmatic effects. In addition, over a hundred quinoline-based drugs are available to treat a variety of disorders. Because of its biological importance, researchers developed one-pot synthetic methods employing effective acid\/base catalysts (Lewis acids, Br\u00f8nsted acids, and ionic liquids), reagents, and transition-metal-based catalysts. These methods have some downsides, including longer reaction times, harsher reaction conditions, creation of byproducts, costly catalysts, use of hazardous solvents, an unacceptable economic yield, and catalyst recovery. Researchers\u2019 focus has switched to creating environmentally friendly and effective methods for the synthesis of quinoline derivatives as a result of these methodologic shortcomings. Because of its special qualities, the use of nanocatalysts or nanocomposites offers an option for the effective synthesis of quinolines. This review focuses on the published research articles on nanocatalysts to synthesize substituted quinoline derivatives. This review covers all contributions until May 2024, focusing on quinoline ring building and mechanistic issues. With the aid of this review, we anticipate that synthetic chemists will be able to develop more effective methods of synthesizing quinolines.<\/jats:p>","DOI":"10.1021\/acsomega.4c07011","type":"journal-article","created":{"date-parts":[[2024,10,14]],"date-time":"2024-10-14T00:45:23Z","timestamp":1728866723000},"page":"42630-42667","source":"Crossref","is-referenced-by-count":41,"title":["Quinoline Synthesis:\nNanocatalyzed Green Protocols\ue5f8An\nOverview"],"prefix":"10.1021","volume":"9","author":[{"given":"Rangappa S.","family":"Keri","sequence":"first","affiliation":[{"name":"Jain (Deemed-to-be University) , , Jain Global Campus, Kanakapura , , ,","place":["Bangalore, Karnataka, India, 562112"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6591-7811","authenticated-orcid":true,"given":"Srinivasa","family":"Budagumpi","sequence":"additional","affiliation":[{"name":"Jain (Deemed-to-be University) , , Jain Global Campus, Kanakapura , , ,","place":["Bangalore, Karnataka, India, 562112"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vinayak","family":"Adimule","sequence":"additional","affiliation":[{"name":"Angadi Institute of Technology and Management (AITM) , Savagaon Road , , ,","place":["Belagavi, Karnataka, India, 5800321"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"316","published-online":{"date-parts":[[2024,10,14]]},"reference":[{"key":"2026081412145908600_cit1","doi-asserted-by":"publisher","DOI":"10.1002\/9781119998372","volume-title":"Heterocycles\nin life and society: An introduction to heterocyclic chemistry, biochemistry\nand applications","author":"Pozharskii","year":"2011","edition":"2"},{"key":"2026081412145908600_cit2","doi-asserted-by":"publisher","DOI":"10.1016\/C2018-0-04877-X","volume-title":"The chemistry\nof heterocycles: Chemistry\nof six to eight membered N, O, S, P and Se heterocycles","author":"Ram","year":"2019"},{"key":"2026081412145908600_cit3","doi-asserted-by":"publisher","DOI":"10.1007\/978-981-19-0832-3","volume-title":"N-Heterocycles\nsynthesis\nand biological evaluation","author":"Ameta","year":"2022"},{"key":"2026081412145908600_cit4","doi-asserted-by":"publisher","first-page":"1161","DOI":"10.1016\/j.biopha.2014.10.007","article-title":"Quinoline:\nA promising antitubercular target","volume":"68","author":"Keri","year":"2014","journal-title":"Biomed. Pharmacother."},{"issue":"5","key":"2026081412145908600_cit5","doi-asserted-by":"publisher","first-page":"476","DOI":"10.1039\/b208140g","article-title":"Quinoline,\nquinazoline, and acridone alkaloids","volume":"20","author":"Michael","year":"2003","journal-title":"Nat. Prod.\nRep."},{"issue":"15","key":"2026081412145908600_cit6","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmech.2021.113865","article-title":"Recent contributions of quinolines to antimalarial\nand anticancer drug discovery research","volume":"226","author":"Van\nde Walle","year":"2021","journal-title":"Eur.\nJ. Med. Chem."},{"key":"2026081412145908600_cit7","doi-asserted-by":"publisher","first-page":"583","DOI":"10.1080\/17460441.2017.1319357","article-title":"An overview\nof quinoline as a privileged scaffold in cancer drug discovery","volume":"12","author":"Musiol","year":"2017","journal-title":"Expet Opin. Drug Discovery"},{"key":"2026081412145908600_cit8","doi-asserted-by":"publisher","first-page":"510","DOI":"10.2174\/1389557518666181018163448","article-title":"A review on quinoline\nderived scaffolds as anti-HIV agents","volume":"19","author":"Chokkar","year":"2019","journal-title":"Mini Rev.\nMed. Chem."},{"key":"2026081412145908600_cit9","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmech.2021.113220","article-title":"Synthetic and medicinal perspective of quinolines as antiviral agents","volume":"215","author":"Kaur","year":"2021","journal-title":"Eur. J. Med. Chem."},{"key":"2026081412145908600_cit10","doi-asserted-by":"publisher","first-page":"389","DOI":"10.1016\/j.drudis.2012.11.003","article-title":"Quinolines: A new hope against inflammation","volume":"18","author":"Mukherjee","year":"2013","journal-title":"Drug Discov Today Off."},{"key":"2026081412145908600_cit11","doi-asserted-by":"publisher","DOI":"10.1016\/j.bioorg.2021.105557","article-title":"Design\nand synthesis\nof ibuprofen-quinoline conjugates as potential anti-inflammatory and\nanalgesic drug candidates","volume":"119","author":"Ghanim","year":"2022","journal-title":"Bioorg. Chem."},{"key":"2026081412145908600_cit12","doi-asserted-by":"publisher","DOI":"10.1016\/j.molstruc.2022.133634","article-title":"A review: Structure-activity\nrelationship and antibacterial\nactivities of quinoline based hybrids","volume":"1268","author":"Patel","year":"2022","journal-title":"J. Mol.\nStruct."},{"key":"2026081412145908600_cit13","doi-asserted-by":"publisher","first-page":"65496","DOI":"10.1039\/C5RA08778C","article-title":"Antihypertensive\nactivity of a quinoline appended chalcone derivative and its site\nspecific binding interaction with a relevant target carrier protein","volume":"5","author":"Kumar","year":"2015","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit14","doi-asserted-by":"publisher","DOI":"10.1016\/j.bioorg.2019.103310","article-title":"Design, synthesis, biological evaluation,\nand molecular modeling studies of quinoline-ferulic acid hybrids as\ncholinesterase inhibitors","volume":"93","author":"Mo","year":"2019","journal-title":"Bioorg. Chem."},{"key":"2026081412145908600_cit15","doi-asserted-by":"publisher","first-page":"843","DOI":"10.2174\/138945006777709557","article-title":"Quinoline\nderivatives as promising inhibitors of antibiotic efflux pump in multidrug\nresistant enterobacter aerogenes isolates","volume":"7","author":"Mahamoud","year":"2006","journal-title":"Curr.\nDrug Targets"},{"key":"2026081412145908600_cit16","doi-asserted-by":"publisher","first-page":"4637","DOI":"10.1016\/j.ejmech.2009.06.031","article-title":"Synthesis and antimicrobial activities\nof novel quinoline derivatives carrying 1,2,4-triazole moiety","volume":"44","author":"Eswaran","year":"2009","journal-title":"Eur. J. Med. Chem."},{"key":"2026081412145908600_cit17","doi-asserted-by":"publisher","first-page":"525","DOI":"10.1007\/s11030-019-09953-4","article-title":"Insights into the current status\nof privileged N-heterocycles\nas antileishmanial agents","volume":"24","author":"Razzaghi-Asl","year":"2020","journal-title":"Mol. Divers."},{"key":"2026081412145908600_cit18","doi-asserted-by":"publisher","first-page":"2522","DOI":"10.1134\/S1070363221120239","article-title":"Novel quinolone derivatives: Synthesis\nand antioxidant\nactivity","volume":"91","author":"Prasad","year":"2021","journal-title":"Russ. J. Gen. Chem."},{"issue":"9","key":"2026081412145908600_cit19","doi-asserted-by":"publisher","first-page":"2164","DOI":"10.1002\/slct.202100115","article-title":"Quinoline:\nA promising scaffold in recent antiprotozoal drug discovery","volume":"6","author":"Dorababu","year":"2021","journal-title":"ChemistrySelect."},{"key":"2026081412145908600_cit20","doi-asserted-by":"publisher","first-page":"196","DOI":"10.1016\/j.ejmech.2017.05.054","article-title":"New quinoline-arylamidine\nhybrids:\nSynthesis, DNA\/RNA binding and tumor activity","volume":"137","author":"Krstulovic\u0301","year":"2017","journal-title":"Eur. J. Med. Chem."},{"key":"2026081412145908600_cit21","doi-asserted-by":"publisher","first-page":"S1980","DOI":"10.1016\/j.arabjc.2013.07.026","article-title":"Molecular modeling\nstudies of quinoline\nderivatives as VEGFR-2 tyrosine kinase inhibitors using pharmacophore\nbased 3D QSAR and docking approach","volume":"10","author":"Ugale","year":"2017","journal-title":"Arab. J.\nChem."},{"key":"2026081412145908600_cit22","doi-asserted-by":"publisher","first-page":"2129","DOI":"10.1021\/jm00040a003","article-title":"A new series\nof PDGF receptor tyrosine kinase inhibitors: 3-substituted quinoline\nderivatives","volume":"37","author":"Maguire","year":"1994","journal-title":"J. Med. Chem."},{"key":"2026081412145908600_cit23","doi-asserted-by":"publisher","first-page":"1445","DOI":"10.1021\/om101037k","article-title":"Oxidatively\nresistant ligands for\npalladium-catalyzed aerobic alcohol oxidation","volume":"30","author":"Pearson","year":"2011","journal-title":"Organomet."},{"key":"2026081412145908600_cit24","doi-asserted-by":"publisher","first-page":"9696","DOI":"10.1016\/j.tet.2005.06.118","article-title":"8-Methylquinoline\npalladacycles: Stable and efficient\ncatalysts for carbon\u2013carbon bond formation","volume":"61","author":"Evans","year":"2005","journal-title":"Tetrahedron"},{"key":"2026081412145908600_cit25","doi-asserted-by":"publisher","first-page":"1883","DOI":"10.1021\/acs.analchem.9b04009","article-title":"Rational design of a targetable fluorescent probe for visualizing\nH2S production under golgi stress response elicited by\nMonensin","volume":"92","author":"Zhu","year":"2020","journal-title":"Anal. Chem."},{"key":"2026081412145908600_cit26","doi-asserted-by":"publisher","DOI":"10.1016\/j.snb.2020.128583","article-title":"A highly selective\nratiometric fluorescence probe for bioimaging\nof hypobromous acid in living cells and zebrafish","volume":"320","author":"Jia","year":"2020","journal-title":"Sens. Actuators B"},{"key":"2026081412145908600_cit27","doi-asserted-by":"publisher","first-page":"122","DOI":"10.1111\/j.1708-8305.1999.tb00843.x","article-title":"Mefloquine\nfor malaria chemoprophylaxis 1992\u20131998: A review","volume":"6","author":"Schlagenhauf","year":"1999","journal-title":"J. Travel Med."},{"key":"2026081412145908600_cit28","doi-asserted-by":"publisher","first-page":"1302","DOI":"10.1039\/b904091a","article-title":"Copper-catalyzed\nazide-alkyne cycloaddition (CuAAC)\nand beyond: New reactivity of copper\u00ad(I) acetylides","volume":"39","author":"Hein","year":"2010","journal-title":"Chem. Soc. Rev."},{"key":"2026081412145908600_cit29","doi-asserted-by":"publisher","first-page":"4874","DOI":"10.1021\/jm501881c","article-title":"Origins\nof the quinolone class of antibacterials: An expanded \u201cdiscovery\nstory","volume":"58","author":"Bisacchi","year":"2015","journal-title":"J. Med. Chem."},{"key":"2026081412145908600_cit30","doi-asserted-by":"publisher","first-page":"13","DOI":"10.2165\/00003495-200262010-00002","article-title":"A critical review\nof the fluoroquinolones","volume":"62","author":"Zhanel","year":"2002","journal-title":"Drugs"},{"key":"2026081412145908600_cit31","doi-asserted-by":"publisher","first-page":"491","DOI":"10.1016\/j.ctrv.2006.07.001","article-title":"Irinotecan\nin the treatment of colorectal\ncancer","volume":"32","author":"Fuchs","year":"2006","journal-title":"Cancer Treat. Rev."},{"key":"2026081412145908600_cit32","doi-asserted-by":"publisher","first-page":"259","DOI":"10.2174\/1574892810666150708110816","article-title":"Cabozantinib\nin thyroid cancer","volume":"10","author":"Fallahi","year":"2015","journal-title":"J. Clin. Oncol."},{"key":"2026081412145908600_cit33","doi-asserted-by":"publisher","first-page":"76","DOI":"10.1007\/s11912-012-0289-x","article-title":"Cabozantinib\nas a novel therapy for renal cell carcinoma","volume":"15","author":"Vaishampayan","year":"2013","journal-title":"Curr. Oncol. Rep."},{"key":"2026081412145908600_cit34","doi-asserted-by":"publisher","first-page":"317","DOI":"10.1007\/s00436-006-0192-1","article-title":"Effects of\ndibucaine on the endocytic\/exocytic\npathways in Trypanosoma cruzi","volume":"99","author":"Souto-Padron","year":"2006","journal-title":"Parasit. Res."},{"issue":"8","key":"2026081412145908600_cit35","doi-asserted-by":"publisher","first-page":"FM01","DOI":"10.7860\/JCDR\/2016\/19052.8286","article-title":"Bedaquiline:\nA novel antitubercular agent for the treatment of multidrug- resistant\ntuberculosis","volume":"10","author":"Yadav","year":"2016","journal-title":"J. Clin. Diag. Res."},{"key":"2026081412145908600_cit36","doi-asserted-by":"publisher","DOI":"10.1002\/14356007.a22_465","article-title":"Quinoline and\nIsoquinoline","volume-title":"Ullmann\u2019s Encyclopedia\nof Industrial Chemistry","author":"Collin","year":"2000"},{"key":"2026081412145908600_cit37","doi-asserted-by":"publisher","first-page":"310","DOI":"10.1002\/jlac.18420420310","article-title":"Untersuchungen\nu\u0308ber die organischen Basen (Investigations of organic bases)","volume":"42","author":"Gerhardt","year":"1842","journal-title":"Annalen der Chemie und Pharmacie"},{"key":"2026081412145908600_cit38","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1002\/047084289X.rq002.pub2","article-title":"Quinoline","volume-title":"Encyclopedia of Reagents for Organic\nSynthesis","author":"Sherman","year":"2001"},{"key":"2026081412145908600_cit39","volume-title":"Application and synthesis\nof small quinoline derivatives","author":"Patel","year":"2023"},{"key":"2026081412145908600_cit40","volume-title":"Various\nsynthesis procedures for quinoline derivatives","author":"Isakhanyan","year":"2020"},{"key":"2026081412145908600_cit41","doi-asserted-by":"publisher","DOI":"10.1002\/9780470638859","volume-title":"Comprehensive organic\nname reactions and reagents","author":"Wang","year":"2010"},{"key":"2026081412145908600_cit42","doi-asserted-by":"publisher","DOI":"10.1155\/2013\/341015","article-title":"Function of nanocatalyst in chemistry of organic compounds\nrevolution: An overview","author":"Hemalatha","year":"2013","journal-title":"J. Nanomat."},{"key":"2026081412145908600_cit43","first-page":"291","volume-title":"Analysis\nand risk of\nnanomaterials in environmental and food samples","author":"Damia","year":"2012"},{"key":"2026081412145908600_cit44","doi-asserted-by":"publisher","first-page":"21","DOI":"10.1007\/978-1-4419-7853-0_2","article-title":"Nanotechnology standards","volume-title":"Nanostructure science and technology","author":"Fred","year":"2011"},{"issue":"10","key":"2026081412145908600_cit45","doi-asserted-by":"publisher","first-page":"3426","DOI":"10.1039\/c3cs60479a","article-title":"Nanomaterials enhanced\nsurface plasmon resonance for biological and chemical sensing applications","volume":"43","author":"Zeng","year":"2014","journal-title":"Chem. Soc. Rev."},{"issue":"1","key":"2026081412145908600_cit46","doi-asserted-by":"publisher","DOI":"10.1088\/0022-3727\/47\/1\/013001","article-title":"Mechanical\nproperties of nanoparticles: basics and\napplications","volume":"47","author":"Guo","year":"2014","journal-title":"J. Phys. D: Appl. Phys."},{"key":"2026081412145908600_cit47","doi-asserted-by":"crossref","DOI":"10.1002\/9783527635993","volume-title":"Homogeneous\ncatalysts: activity, stability, deactivation","author":"van Leeuwen","year":"2011"},{"key":"2026081412145908600_cit48","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.progsolidstchem.2006.03.001","article-title":"Size dependence\nof nanostructures: Impact of bond order deficiency","volume":"35","author":"Sun","year":"2007","journal-title":"Prog. Solid State Chem."},{"key":"2026081412145908600_cit49","doi-asserted-by":"publisher","first-page":"743","DOI":"10.1039\/b921171c","article-title":"Green chemistry\nby nano-catalysis","volume":"12","author":"Polshettiwar","year":"2010","journal-title":"Green Chem."},{"key":"2026081412145908600_cit50","volume-title":"Nanomaterials\nin Catalysis","author":"Somorjai","year":"2012","edition":"1"},{"key":"2026081412145908600_cit51","doi-asserted-by":"publisher","first-page":"20373","DOI":"10.1039\/D3RA03646D","article-title":"Reusable nano-catalyzed\ngreen protocols for the synthesis of quinoxalines: An overview","volume":"13","author":"Keri","year":"2023","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit52","doi-asserted-by":"publisher","DOI":"10.1007\/s11244-022-01562-0","article-title":"The nano-based catalyst\nfor the synthesis of benzimidazoles","author":"Keri","year":"2013","journal-title":"Top. Catal."},{"key":"2026081412145908600_cit53","doi-asserted-by":"publisher","first-page":"218","DOI":"10.1016\/j.catcom.2012.05.022","article-title":"(\u03b1-Fe2O3)-MCM-41 as a magnetically recoverable nanocatalyst\nfor the synthesis of pyrazolo\u00ad[4,3-c]\u00adpyridines at\nroom temperature","volume":"26","author":"Rostamizadeh","year":"2012","journal-title":"Catal. Comm."},{"key":"2026081412145908600_cit54","doi-asserted-by":"publisher","first-page":"111","DOI":"10.1002\/jhet.692","article-title":"MCM-41-SO3H as a nanoreactor\nfor the one-pot,solvent-free synthesis of 1, 8-dioxo-9-aryl\ndecahydroacridines","volume":"49","author":"Rostamizadeh","year":"2012","journal-title":"J. Heterocyclic Chem."},{"key":"2026081412145908600_cit55","doi-asserted-by":"publisher","first-page":"1033","DOI":"10.3987\/COM-11-S(P)81","article-title":"Multicomponent click\nsynthesis of potentially biologically active triazoles catalysed by\ncopper nanoparticles on activated carbon in water","volume":"84","author":"Alonso","year":"2012","journal-title":"Heterocycles"},{"key":"2026081412145908600_cit56","doi-asserted-by":"publisher","first-page":"615","DOI":"10.1007\/s12039-011-0133-0","article-title":"ZnO nanoparticle\nas catalyst for efficient green one-pot synthesis of coumarins through\nKnoevenagel condensation","volume":"123","author":"Kumar","year":"2011","journal-title":"J. Chem. Sci."},{"key":"2026081412145908600_cit57","doi-asserted-by":"publisher","first-page":"1419","DOI":"10.1016\/j.cclet.2011.06.003","article-title":"CuO nanoparticles:\nan efficient and recyclable nanocatalyst\nfor the rapid and green synthesis of 3,4-dihydropyrano\u00ad[c]\u00adchromenes","volume":"22","author":"Mehrabi","year":"2011","journal-title":"Chin. Chem. Lett."},{"key":"2026081412145908600_cit58","doi-asserted-by":"publisher","first-page":"7827","DOI":"10.1016\/j.tet.2012.07.034","article-title":"Fe3O4\/SiO2 nanoparticles: an efficient and magnetically\nrecoverable nanocatalyst for the one-potmulticomponent synthesis of\ndiazepines","volume":"68","author":"Maleki","year":"2012","journal-title":"Tetrahedron"},{"key":"2026081412145908600_cit59","doi-asserted-by":"publisher","DOI":"10.1515\/hc-2022-0171","article-title":"Inorganic\nnanoparticles promoted\nsynthesis of oxygen-containing heterocycles","volume":"30","author":"Devi","year":"2024","journal-title":"Heterocyc. Comm."},{"issue":"30","key":"2026081412145908600_cit60","doi-asserted-by":"publisher","first-page":"19640","DOI":"10.1039\/D2RA03122A","article-title":"Nanocatalysts: applications for the\nsynthesis of N-containing five-membered heterocycles","volume":"12","author":"Jangir","year":"2022","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit61","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.jsps.2012.03.002","article-title":"Quinoline: A versatile\nheterocyclic","volume":"21","author":"Marella","year":"2013","journal-title":"Saudi Pharm. J."},{"key":"2026081412145908600_cit62","doi-asserted-by":"publisher","first-page":"587","DOI":"10.1016\/j.ejps.2017.08.027","article-title":"Amino acid\nor peptide conjugates of acridine\/acridone and quinoline\/quinolone-containing\ndrugs. A critical examination of their clinical effectiveness within\na twenty-year timeframe in antitumor chemotherapy and treatment of\ninfectious diseases","volume":"109","author":"Kukowska","year":"2017","journal-title":"Eur. J. Pharma. Sci."},{"key":"2026081412145908600_cit63","doi-asserted-by":"publisher","first-page":"22","DOI":"10.1016\/j.ejmech.2017.07.061","article-title":"Quinoline\nhybrids and their antiplasmodial and antimalarial\nactivities","volume":"139","author":"Hu","year":"2017","journal-title":"Eur. J. Med. Chem."},{"key":"2026081412145908600_cit64","doi-asserted-by":"publisher","first-page":"871","DOI":"10.1016\/j.ejmech.2014.07.044","article-title":"A review on\nanticancer potential\nof bioactive heterocycle quinoline","volume":"97","author":"Afzal","year":"2015","journal-title":"Eur. J.\nMed. Chem."},{"key":"2026081412145908600_cit65","doi-asserted-by":"publisher","first-page":"354","DOI":"10.1016\/j.bjbas.2017.07.005","article-title":"A review on quinoline hydrazone derivatives as a new\nclass of potent antitubercular and anticancer agents","volume":"6","author":"Mandewale","year":"2017","journal-title":"Beni-Suef Uni. J. Basi.Appl. Sci."},{"issue":"11","key":"2026081412145908600_cit66","doi-asserted-by":"publisher","first-page":"4920","DOI":"10.1016\/j.arabjc.2016.10.009","article-title":"Comprehensive review\non current developments of quinoline-based\nanticancer agents","volume":"12","author":"Jain","year":"2019","journal-title":"Ara. J. Chem."},{"key":"2026081412145908600_cit67","doi-asserted-by":"publisher","first-page":"42020","DOI":"10.1039\/C5RA07798B","article-title":"Metal-free domino one-pot protocols\nfor quinoline synthesis","volume":"5","author":"Bharate","year":"2015","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit68","doi-asserted-by":"publisher","first-page":"24463","DOI":"10.1039\/C4RA01814A","article-title":"Recent\nadvances in thesynthesis of quinolines: A review","volume":"4","author":"Prajapati","year":"2014","journal-title":"RSC Adv."},{"issue":"8","key":"2026081412145908600_cit69","doi-asserted-by":"publisher","first-page":"4064","DOI":"10.1021\/acssuschemeng.6b01010","article-title":"Synthesis of quinolines: A green\nperspective","volume":"4","author":"Batista","year":"2016","journal-title":"Sustainable Chem. Eng."},{"issue":"22","key":"2026081412145908600_cit70","doi-asserted-by":"publisher","DOI":"10.1002\/slct.202201059","article-title":"Environmentally\nbenign approaches towards the synthesis of quinolines","volume":"7","author":"Kumar","year":"2022","journal-title":"ChemistrySelect"},{"issue":"7","key":"2026081412145908600_cit71a","doi-asserted-by":"publisher","first-page":"631","DOI":"10.2174\/1570193X15666181001142122","article-title":"Review\non the role of the metal catalysts in the synthesis of pharmacologically\nimportant quinoline substrate","volume":"16","author":"Mahajan","year":"2019","journal-title":"Mini-Rev. Org.\nChem."},{"key":"2026081412145908600_cit71b","doi-asserted-by":"publisher","first-page":"121","DOI":"10.1016\/j.ejmech.2018.11.026","article-title":"Green recipes to quinoline: A review","volume":"164","author":"Nainwal","year":"2019","journal-title":"Eur. J. Med. Chem."},{"key":"2026081412145908600_cit72a","doi-asserted-by":"publisher","first-page":"2339","DOI":"10.1039\/D4OB00034J","article-title":"A. Recent advancement\nin the synthesis of quinoline derivatives via multicomponent reactions","volume":"22","author":"Mandal","year":"2024","journal-title":"Org. Biomol. Chem."},{"key":"2026081412145908600_cit72b","doi-asserted-by":"publisher","first-page":"337","DOI":"10.1080\/17518253.2022.2064194","article-title":"A review\non synthetic investigation for quinoline- recent green approaches","volume":"15","author":"Patel","year":"2022","journal-title":"Green Chem. Lett. Rev."},{"issue":"5","key":"2026081412145908600_cit72c","doi-asserted-by":"publisher","first-page":"671","DOI":"10.2174\/1570179416666190719112423","article-title":"Recent Progress in the Synthesis of Quinolines","volume":"16","author":"Xuan","year":"2019","journal-title":"Curr. Org. Synth."},{"key":"2026081412145908600_cit72d","doi-asserted-by":"publisher","DOI":"10.3389\/fchem.2022.1074331","article-title":"Recent advances in functionalized quinoline scaffolds\nand hybrids\ue5f8Exceptional pharmacophore in therapeutic medicine","volume":"10","author":"Elebiju","year":"2023","journal-title":"Front. Chem."},{"key":"2026081412145908600_cit72e","doi-asserted-by":"publisher","first-page":"18594","DOI":"10.1039\/D2RA02896D","article-title":"Recent advances\nin chemistry and therapeutic potential of functionalized quinoline\nmotifs \u2013 a review","volume":"12","author":"Ajani","year":"2022","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit72f","doi-asserted-by":"publisher","first-page":"2443","DOI":"10.1007\/s00044-023-03121-y","article-title":"Current progress toward synthetic routes and medicinal\nsignificance of quinoline","volume":"32","author":"Shehab","year":"2023","journal-title":"Med. Chem. Res."},{"key":"2026081412145908600_cit73a","volume-title":"The iron oxides: Structure, properties, reactions,\noccurences\nand uses","author":"Cornell","year":"2006","edition":"2nd"},{"key":"2026081412145908600_cit73b","doi-asserted-by":"publisher","first-page":"4432","DOI":"10.1166\/jnn.2017.14195","article-title":"Recent advances on Fe-based magnetic\nnanoparticles in organic transformations","volume":"17","author":"Payra","year":"2017","journal-title":"J.\nNanosci. Nanotechnol."},{"key":"2026081412145908600_cit74a","doi-asserted-by":"publisher","first-page":"7579","DOI":"10.1039\/D4GC01870B","article-title":"A review on\nsustainable iron oxide nanoparticles: syntheses and applications in\norganic catalysis and environmental remediation Check for updates","volume":"26","author":"Chaudhari","year":"2024","journal-title":"Green Chem."},{"key":"2026081412145908600_cit74b","doi-asserted-by":"publisher","first-page":"3462","DOI":"10.3390\/nano12193462","article-title":"Recent Advances in Carbon-Based Iron\nCatalysts for Organic Synthesis","volume":"12","author":"Wang","year":"2022","journal-title":"Nanomaterials"},{"key":"2026081412145908600_cit74c","doi-asserted-by":"publisher","DOI":"10.1016\/j.tet.2022.132641","article-title":"Magnetically active iron oxide nanoparticles for catalysis\nof organic transformations: A review","volume":"106\u2013107","author":"Kumar","year":"2022","journal-title":"Tetrahedron"},{"key":"2026081412145908600_cit74d","doi-asserted-by":"publisher","first-page":"831","DOI":"10.3390\/ma11050831","article-title":"Fe-Based Nano-Materials in Catalysis","volume":"11","author":"Theofanidis","year":"2018","journal-title":"Materials"},{"key":"2026081412145908600_cit75","doi-asserted-by":"publisher","DOI":"10.1016\/j.poly.2019.114148","article-title":"Synthesis of Fe3O4@SiO2\/isoniazid\/Cu\u00ad(II) magnetic nanocatalyst as\na recyclable catalyst for a highly efficient preparation of quinolines\nin moderate conditions","volume":"173","author":"Lotfi","year":"2019","journal-title":"Polyhedron"},{"key":"2026081412145908600_cit76","doi-asserted-by":"publisher","first-page":"219","DOI":"10.1016\/j.jfluchem.2015.08.007","article-title":"Preparation\nof trifluoroacetic acid-immobilized Fe3O4@SiO2\u2013APTES nanocatalyst for synthesis of quinolines","volume":"178","author":"Jafarzadeh","year":"2015","journal-title":"J. Flu. Chem."},{"key":"2026081412145908600_cit77","doi-asserted-by":"publisher","DOI":"10.1016\/j.clay.2020.105841","article-title":"Magnetic \u03b3-Fe2O3@Cu-LDH intercalated with palladium cysteine:\nAn efficient\ndual nano catalyst in tandem CeN coupling and cyclization progress\nof synthesis quinolones","volume":"198","author":"Esfandiary","year":"2020","journal-title":"Appl. Clay Sci."},{"key":"2026081412145908600_cit78","doi-asserted-by":"publisher","DOI":"10.1016\/j.mcat.2020.110924","article-title":"Synthesis\nand characterization of\nFe3O4@SiO2@(CH2)3NH\u00ad(CH2)2O2P\u00ad(OH)2 and\nits catalytic application in the synthesis of benzo-[h]\u00adquinoline-4-carboxylic\nacids via a cooperative anomeric based oxidation\nmechanism","volume":"489","author":"Karimi","year":"2020","journal-title":"Mol. Catal."},{"issue":"12","key":"2026081412145908600_cit79","doi-asserted-by":"publisher","first-page":"4181","DOI":"10.1002\/jhet.4125","article-title":"Synthesis\nof benzo\u00ad[h]\u00adquinolone and\nbenzo\u00ad[c]\u00adacridinone derivatives by Fe3O4@PS-Arginine\u00ad[HSO4] as an efficient magnetic nanocatalyst","volume":"57","author":"Karkhah","year":"2020","journal-title":"J. Hetero Chem."},{"key":"2026081412145908600_cit80","doi-asserted-by":"publisher","first-page":"16327","DOI":"10.1039\/C5CC05752C","article-title":"Aggregates\nof Perylene bisimide stabilized\nsuperparamagnetic Fe3O4 nanoparticles: An efficient\ncatalyst for the preparation of propargylamines and quinolines via C-H activation","volume":"51","author":"Kaur","year":"2015","journal-title":"Chem. Commun."},{"issue":"5","key":"2026081412145908600_cit81","doi-asserted-by":"publisher","first-page":"269","DOI":"10.1515\/znb-2017-0200","article-title":"Synthesis\nof hexahydro-4-phenylquinoline-3-carbonitriles\nusing Fe3O4@SiO2-SO3H nanoparticles\nas a superior and retrievable heterogeneous catalyst under ultrasonic\nirradiations","volume":"73","author":"Safaei-Ghomi","year":"2018","journal-title":"Z. Naturforsch."},{"key":"2026081412145908600_cit82","doi-asserted-by":"publisher","first-page":"1339","DOI":"10.1007\/s00706-014-1368-5","article-title":"Fe3O4 nano-particles\nsupported on cellulose as an efficient catalystfor the synthesis of\npyrimido\u00ad[4,5-b]\u00adquinolines in water","volume":"146","author":"Edjlali","year":"2015","journal-title":"Monatsh.\nChem."},{"key":"2026081412145908600_cit83","doi-asserted-by":"publisher","first-page":"55","DOI":"10.1016\/j.jorganchem.2019.05.020","article-title":"Fe3-xTixO4-supported sulfamic acid nanoparticles: New\nmagnetic nanocatalyst for the synthesis of hexahydroquinolines","volume":"895","author":"Azarifar","year":"2019","journal-title":"Journal of Organometallic Chemistry"},{"key":"2026081412145908600_cit84","doi-asserted-by":"publisher","first-page":"648","DOI":"10.1515\/chem-2020-0063","article-title":"Fe3O4@urea\/HITh-SO3H as an efficient and\nreusable catalyst for the solvent-free\nsynthesis of 7-aryl-8H-benzo\u00ad[h]\u00adindeno-[1,2-b]\u00adquinoline-8-one and indeno\u00ad[2\u2032,1\u2032:5,6]\u00adpyrido\u00ad[2,3-d]\u00adpyrimidine\nderivatives","volume":"18","author":"Jiang","year":"2020","journal-title":"Open Chem."},{"key":"2026081412145908600_cit85","doi-asserted-by":"publisher","first-page":"5887","DOI":"10.1007\/s11164-015-2411-9","article-title":"Imidazole-functionalized magnetic\nFe3O4 nanoparticles: an efficient, green, recyclable\ncatalyst for\none-pot Friedla\u0308nder quinoline synthesis","volume":"42","author":"Rezayati","year":"2016","journal-title":"Res. Chem. Intermed."},{"key":"2026081412145908600_cit86","doi-asserted-by":"publisher","first-page":"805","DOI":"10.1007\/s13738-020-02069-9","article-title":"Magnetite\n(Fe3O4) nanoparticles-supported dodecylbenzenesulfonic\nacid\nas a highly efficient and green heterogeneous catalyst for the synthesis\nof substituted quinolines and 1-amidoalkyl-2-naphthol derivatives","volume":"18","author":"Katheriya","year":"2021","journal-title":"J. Ira. Chem. Soc."},{"issue":"7","key":"2026081412145908600_cit87","doi-asserted-by":"publisher","first-page":"3207","DOI":"10.1021\/acsomega.9b03277","article-title":"Ionically tagged magnetic nanoparticles with urea linkers:\nApplication for preparation of 2-aryl-quinoline-4-carboxylic acids via an anomeric-based oxidation mechanism","volume":"5","author":"Ghasemi","year":"2020","journal-title":"ACS Omega"},{"key":"2026081412145908600_cit88","doi-asserted-by":"publisher","first-page":"3012","DOI":"10.1039\/C9NJ05468E","article-title":"Praseodymium\n(III) anchored on the\nCoFe2O4 MNPs: An efficient heterogeneous magnetic\nnanocatalyst for one-pot, multi-component domino synthesis of polyhydroquinoline\nand 2,3-dihydroquinazolin-4\u00ad(1H)-one derivatives","volume":"44","author":"Tamoradi","year":"2020","journal-title":"New J. Chem."},{"key":"2026081412145908600_cit89","doi-asserted-by":"publisher","first-page":"421","DOI":"10.1007\/s11030-018-9887-3","article-title":"RuIII@CMC\/Fe3O4 hybrid: An efficient,magnetic, retrievable,self-organized\nnanocatalyst for green synthesis of pyranopyrazole and polyhydroquinoline\nderivatives","volume":"23","author":"Chen","year":"2019","journal-title":"Mol. Divers."},{"key":"2026081412145908600_cit90","doi-asserted-by":"publisher","first-page":"64","DOI":"10.2174\/1386207319666161223121612","article-title":"Magnetite\nnanoparticles-supported APTES as a powerful and recoverable nanocatalyst\nfor the preparation of 2-amino-5,10-dihydro-5,10-dioxo-4H-benzo\u00ad[g]\u00adchromenes and tetrahydrobenzo\u00ad[g]\u00adquinoline-5,10-diones","volume":"20","author":"Ghasemzadeh","year":"2017","journal-title":"Comb. Chem. High. T.\nScr."},{"key":"2026081412145908600_cit91","doi-asserted-by":"publisher","first-page":"6234","DOI":"10.1021\/cr300527g","article-title":"Aerobic\ncopper-catalyzed organic reactions","volume":"113","author":"Allen","year":"2013","journal-title":"Chem. Rev."},{"key":"2026081412145908600_cit92a","doi-asserted-by":"publisher","first-page":"3722","DOI":"10.1021\/acs.chemrev.5b00482","article-title":"Cu and Cu-based nanoparticles: Synthesis\nand applications in catalysis","volume":"116","author":"Gawande","year":"2016","journal-title":"Chem. Rev."},{"key":"2026081412145908600_cit92b","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.ccr.2017.10.004","article-title":"Copper nanoparticles as inexpensive\nand efficient catalyst: A valuable contribution in organic synthesis","volume":"353","author":"Ojha","year":"2017","journal-title":"Coord. Chem. Rev."},{"key":"2026081412145908600_cit93a","doi-asserted-by":"publisher","first-page":"6169","DOI":"10.1007\/s10853-024-09546-z","article-title":"A review on copper-based nanoparticles as a catalyst:\nsynthesis and applications in coupling reactions","volume":"59","author":"Pathak","year":"2024","journal-title":"J. Mater. Sci."},{"key":"2026081412145908600_cit93b","doi-asserted-by":"publisher","DOI":"10.1149\/2162-8777\/ac07f8","article-title":"Review\ue5f8Multifunctional Copper\nNanoparticles: Synthesis and Applications","volume":"10","author":"Bhagat","year":"2021","journal-title":"ECS\nJ. Solid State Sci. Technol."},{"key":"2026081412145908600_cit94","doi-asserted-by":"publisher","first-page":"15154","DOI":"10.1039\/c3ra47212d","article-title":"Recyclable nano\ncopper oxide catalyzed\nsynthesis of quinoline-2,3-dicarboxylates under ligand free conditions","volume":"4","author":"Venkanna","year":"2014","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit95","doi-asserted-by":"publisher","first-page":"11480","DOI":"10.1039\/D3RA01164J","article-title":"CuI nanoparticle-immobilized\non a\nhybrid material composed of IRMOF-3 and a sulfonamide-based porous\norganic polymer as an efficient nanocatalyst for one-pot synthesis\nof 2,4-diarylquinolines","volume":"13","author":"Koosha","year":"2023","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit96","doi-asserted-by":"publisher","first-page":"11624","DOI":"10.1039\/c3ra46119j","article-title":"CuFe2O4 nanoparticles: a magnetically\nrecoverable and reusable catalyst for the synthesis of quinoline and\nquinazoline derivatives in aqueous media","volume":"4","author":"Baghbanian","year":"2014","journal-title":"RSC\nAdv."},{"key":"2026081412145908600_cit97","doi-asserted-by":"publisher","first-page":"2832","DOI":"10.1002\/adsc.201700535","article-title":"Making copper(0)\nnanoparticles in glycerol: a straightforward synthesis for a multipurpose\ncatalyst","volume":"359","author":"Dang-Bao","year":"2017","journal-title":"Adv. Synth. Catal."},{"key":"2026081412145908600_cit98","doi-asserted-by":"publisher","first-page":"4422","DOI":"10.1002\/adsc.202100631","article-title":"Cascade reaction of\n\u03b1, \u03b2-unsaturated ketones and 2-aminoaryl\nalcohols for the synthesis of 3-acylquinolines by a copper nanocatalyst","volume":"363","author":"Liu","year":"2021","journal-title":"Adv. Synth. Catal."},{"key":"2026081412145908600_cit99","doi-asserted-by":"publisher","first-page":"1017","DOI":"10.1016\/j.jcat.2022.08.009","article-title":"CuO NPs catalyzed\nsynthesis of quinolines, pyridines, and pyrroles via dehydrogenative coupling strategy","volume":"413","author":"Gupta","year":"2022","journal-title":"J. Catal."},{"key":"2026081412145908600_cit100","doi-asserted-by":"publisher","first-page":"3853","DOI":"10.5012\/bkcs.2011.32.11.3853","article-title":"CuO nanoparticles\nas an efficient and reusable catalyst for the one-pot Friedlander\nquinoline synthesis","volume":"32","author":"Nezhad","year":"2011","journal-title":"Bull. Korean Chem. Soc."},{"key":"2026081412145908600_cit101","doi-asserted-by":"publisher","first-page":"243","DOI":"10.7508\/JNS.2011.03.009","article-title":"Nanocrystalline\ncopper\u00ad(II) oxide-catalyzed\none-pot four component synthesis of polyhydroquinoline derivatives\nunder solvent-free conditions","volume":"1","author":"Safaei-Ghomi","year":"2012","journal-title":"J. Nano Str."},{"key":"2026081412145908600_cit102","doi-asserted-by":"publisher","first-page":"890","DOI":"10.1166\/jnn.2020.16923","article-title":"Chitosan decorated copper nanoparticles as efficient\ncatalyst for synthesis of novel quinoline derivatives","volume":"20","author":"Alghamdi","year":"2020","journal-title":"J. Nanosci. Nanotechnol."},{"issue":"5","key":"2026081412145908600_cit103","doi-asserted-by":"publisher","first-page":"3306","DOI":"10.1039\/C4RA13299H","article-title":"Zinc oxide based\nphotocatalysis:\ntailoring surface-bulk structure and related interfacial charge carrier\ndynamics for better environmental applications","volume":"5","author":"Kumar","year":"2015","journal-title":"RSC Adv."},{"issue":"25","key":"2026081412145908600_cit104","doi-asserted-by":"publisher","first-page":"R829","DOI":"10.1088\/0953-8984\/16\/25\/R01","article-title":"Zinc oxide\nnanostructures: growth, properties and applications","volume":"16","author":"Wang","year":"2004","journal-title":"J. Phys.: Condens. Matter"},{"issue":"2","key":"2026081412145908600_cit105","doi-asserted-by":"publisher","first-page":"2492","DOI":"10.1016\/j.ceramint.2014.10.069","article-title":"Plectranthus\namboinicus leaf extract-assisted\nbiosynthesis of ZnO nanoparticles and their photocatalytic activity","volume":"41","author":"Fu","year":"2015","journal-title":"Ceram. Int."},{"key":"2026081412145908600_cit106","doi-asserted-by":"publisher","first-page":"223","DOI":"10.1016\/j.mseb.2017.09.023","article-title":"Sonochemical\nsynthesis of ZnO nanoparticles and its use as photocatalyst in H2\ngeneration","volume":"226","author":"Lue\u0301vano-Hipo\u0301lito","year":"2017","journal-title":"Mater. Sci. Eng. B"},{"issue":"4","key":"2026081412145908600_cit107","doi-asserted-by":"publisher","first-page":"581","DOI":"10.1007\/s13204-015-0472-0","article-title":"Synthesis,\ncharacterization, and evaluation of the antimicrobial efficacy of Boswellia ovalifoliolata stem bark-extract-mediated zinc\noxide nanoparticles","volume":"6","author":"Supraja","year":"2016","journal-title":"Appl. Nanosci"},{"key":"2026081412145908600_cit108a","doi-asserted-by":"publisher","first-page":"631","DOI":"10.1016\/j.mattod.2017.11.003","article-title":"ZnO tetrapod materials\nfor functional applications","volume":"21","author":"Mishra","year":"2018","journal-title":"Mater. Today"},{"key":"2026081412145908600_cit108b","doi-asserted-by":"publisher","DOI":"10.1002\/slct.202303181","article-title":"Zinc Oxide\nNanoparticles as Efficient Heterogeneous Catalyst for Synthesis of\nBio-active Heterocyclic Compounds","volume":"8","author":"Kumar","year":"2023","journal-title":"Chemistry\nselect"},{"key":"2026081412145908600_cit109","doi-asserted-by":"publisher","first-page":"389","DOI":"10.1007\/s40097-017-0247-0","article-title":"Recent developments on nano-ZnO catalyzed\nsynthesis\nof bioactive heterocycles","volume":"7","author":"Banerjee","year":"2017","journal-title":"J. Nanostruct. Chem."},{"key":"2026081412145908600_cit110","doi-asserted-by":"publisher","DOI":"10.1016\/j.jece.2021.106879","article-title":"Enhanced catalytic performance of\nZnO\/carbon materials\nin the green synthesis of poly-substituted quinolines","volume":"10","author":"Godino-Ojer","year":"2022","journal-title":"J. Envir. Chem. Eng."},{"key":"2026081412145908600_cit111","doi-asserted-by":"publisher","first-page":"S119","DOI":"10.1007\/BF03254288","article-title":"Synthesis of quinolines using nano-flake\nZnO as a new\ncatalyst under solvent-free conditions","volume":"8","author":"Hosseini-Sarvari","year":"2011","journal-title":"J. Iran.\nChem. Soc."},{"key":"2026081412145908600_cit112","first-page":"1548","article-title":"A simple and green\nsynthesis of highly functionalized quinoline derivatives using zinc\noxide nanoparticles","volume":"55B","author":"Valekar","year":"2016","journal-title":"Indian J. Chem."},{"key":"2026081412145908600_cit113","doi-asserted-by":"publisher","first-page":"1654","DOI":"10.1016\/j.tetlet.2015.02.030","article-title":"Heterogeneous bimetallic\nZnFe2O4\nnanopowder catalysed facile four component reaction for the synthesis\nof spiro\u00ad[indoline-3,20- quinoline] derivatives from isatins in water\nmedium","volume":"56","author":"Debnath","year":"2015","journal-title":"Tetrahedron Lett."},{"key":"2026081412145908600_cit114a","doi-asserted-by":"publisher","DOI":"10.1038\/s41598-020-69679-4","article-title":"Synthesis of nickel nanoparticles by a green and convenient\nmethod as a magnetic mirror with antibacterial activities","volume":"10","author":"Ahghari","year":"2020","journal-title":"Sci. Rep."},{"issue":"1","key":"2026081412145908600_cit114b","doi-asserted-by":"publisher","first-page":"1456","DOI":"10.1515\/ntrev-2020-0109","article-title":"Advanced nickel nanoparticles technology:\nFrom synthesis to applications","volume":"9","author":"Jaji","year":"2020","journal-title":"Nanotechnol.\nRev."},{"issue":"19","key":"2026081412145908600_cit115","doi-asserted-by":"publisher","first-page":"2906","DOI":"10.1080\/00397911.2020.1789168","article-title":"Synthesis\nof heterocycles using nanomagnetic nickel catalysts","volume":"50","author":"Ashraf","year":"2020","journal-title":"Syn. Comm."},{"key":"2026081412145908600_cit116","doi-asserted-by":"publisher","first-page":"210","DOI":"10.1016\/j.apcata.2006.10.027","article-title":"Ni-nanoparticles:\nA\nmild chemo-selective catalyst for synthesis of thioethers","volume":"317","author":"Saxena","year":"2007","journal-title":"Appl. Catal. A: Gen."},{"key":"2026081412145908600_cit117","doi-asserted-by":"publisher","first-page":"212","DOI":"10.1016\/j.clay.2010.12.025","article-title":"Ni nanoparticles supported\non microwave-synthesised saponite for the hydrogenation of styrene\noxide","volume":"53","author":"Vicente","year":"2011","journal-title":"Appl. Clay. Sci."},{"key":"2026081412145908600_cit118","doi-asserted-by":"publisher","first-page":"4161","DOI":"10.1016\/j.tetlet.2006.04.048","article-title":"Ni-nanoparticles: an efficient green\ncatalyst for chemoselective\nreduction of aldehydes","volume":"47","author":"Kidwai","year":"2006","journal-title":"Tetrahedron."},{"key":"2026081412145908600_cit119","doi-asserted-by":"publisher","first-page":"1847","DOI":"10.1016\/j.tet.2007.11.093","article-title":"Hydrogen transfer\nreduction\nof carbonyl compounds promoted by nickel(0) nanoparticles","volume":"64","author":"Alonso","year":"2008","journal-title":"Tetrahedron."},{"key":"2026081412145908600_cit120","doi-asserted-by":"publisher","first-page":"2279","DOI":"10.1016\/j.jssc.2009.05.036","article-title":"Decorating multi-walled carbon nanotubes\nwith nickel nanoparticles for selective hydrogenation of citral","volume":"182","author":"Tang","year":"2009","journal-title":"J. Solid State Chem."},{"key":"2026081412145908600_cit121","doi-asserted-by":"publisher","first-page":"35","DOI":"10.1016\/j.molcata.2006.12.042","article-title":"Ni-nanoparticles: An\nefficient green catalyst for chemo-selective oxidative coupling of\nthiols","volume":"269","author":"Saxena","year":"2007","journal-title":"J. Mol. Catal. A: Chem."},{"key":"2026081412145908600_cit122","doi-asserted-by":"publisher","first-page":"45599","DOI":"10.1039\/C5RA06593C","article-title":"Nickel nanoparticles:\na highly efficient\nand retrievable catalyst for the solventless Friedlander annulation\nof quinolines and their in silico molecular docking studies as histone\ndeacetylase inhibitors","volume":"5","author":"Angajala","year":"2015","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit123","doi-asserted-by":"publisher","first-page":"1595","DOI":"10.1016\/j.cclet.2014.06.026","article-title":"Nickel oxide nanoparticles catalyzed synthesis of poly-substituted\nquinolines via Friedlander hetero-annulation reaction","volume":"25","author":"Palakshi Reddy","year":"2014","journal-title":"Chin. Chem. Lett."},{"key":"2026081412145908600_cit124","doi-asserted-by":"publisher","first-page":"978","DOI":"10.1002\/aoc.3530","article-title":"A green biosynthesis\nof NiO nanoparticles using aqueous extract of Tamarix serotina and\ntheir characterization and application","volume":"30","author":"Nasseri","year":"2016","journal-title":"Appl.\nOrganometalic Chem."},{"key":"2026081412145908600_cit125","doi-asserted-by":"publisher","first-page":"1754","DOI":"10.1016\/j.tetlet.2009.01.140","article-title":"Nickel\nnanoparticle-catalyzed facile and efficient one-pot synthesis of polyhydroquinoline\nderivatives via Hantzsch condensation under solvent-free\nconditions","volume":"50","author":"Sapkal","year":"2009","journal-title":"Tetrahedron Lett."},{"key":"2026081412145908600_cit126","doi-asserted-by":"publisher","first-page":"8289","DOI":"10.1039\/D0NJ00223B","article-title":"Synthesis\nof new Ni complex supported on CoFe2O4 and its\napplication as an efficient and green catalyst for the synthesis of\nbis\u00ad(pyrazolyl)\u00admethane and polyhydroquinoline derivatives","volume":"44","author":"Tamoradi","year":"2020","journal-title":"New J. Chem."},{"key":"2026081412145908600_cit127","doi-asserted-by":"publisher","first-page":"8268","DOI":"10.1039\/D3NJ00988B","article-title":"A sustainable approach\nfor nickel nanoparticles synthesis: expeditious access to N-heterocycles\nunder heterogeneous condition and photophysical studies","volume":"47","author":"Thrilokraj","year":"2023","journal-title":"New J. Chem."},{"key":"2026081412145908600_cit128","doi-asserted-by":"publisher","first-page":"8197","DOI":"10.1021\/acscatal.1c01561","article-title":"Tuning the catalytic performance\nof cobalt nanoparticles by tungsten doping for efficient and selective\nhydrogenation of quinolines under mild conditions","volume":"11","author":"Puche","year":"2021","journal-title":"ACS Catal."},{"key":"2026081412145908600_cit129","doi-asserted-by":"publisher","first-page":"150","DOI":"10.1002\/cmmi.241","article-title":"Cobalt nanoparticles\nas a novel magnetic resonance contrast agent-relaxivities at 1.5 and\n3 T","volume":"3","author":"Parkes","year":"2008","journal-title":"Contrast Media Mol. Imaging"},{"key":"2026081412145908600_cit130","doi-asserted-by":"publisher","first-page":"593","DOI":"10.1007\/s11664-007-0112-x","article-title":"Magnetic Nanocomposite\nfor Potential Ultrahigh Frequency\nMicroelectronic Application","volume":"36","author":"Dong","year":"2007","journal-title":"J. Electron. Mater."},{"key":"2026081412145908600_cit131","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1007\/s13205-020-02230-4","article-title":"Preparation,\ncharacterization, and anticancer efficacy\nof novel cobalt oxide nanoparticles conjugated with thiosemicarbazide","volume":"10","author":"Jarestan","year":"2020","journal-title":"Biotech"},{"key":"2026081412145908600_cit132","doi-asserted-by":"publisher","DOI":"10.1016\/j.matpr.2023.06.178","article-title":"Catalytic applications\nof cobalt\/cobalt oxide nanoparticles in heterocyclic compounds","author":"Kharat","year":"2023","journal-title":"Matet.Today: Proc."},{"key":"2026081412145908600_cit133","doi-asserted-by":"publisher","first-page":"6768","DOI":"10.1039\/D0NJ05767C","article-title":"The preparation\nof a Co@C3N4 catalyst and applications in the synthesis of quinolines\nfrom 2-aminobenzyl alcohols with ketones","volume":"45","author":"Cao","year":"2021","journal-title":"New\nJ. Chem."},{"key":"2026081412145908600_cit134","doi-asserted-by":"publisher","first-page":"239","DOI":"10.1016\/j.jcat.2020.01.034","article-title":"Selective reductive\nannulation reaction for direct synthesis of functionalized quinolines\nby a cobalt nanocatalyst","volume":"383","author":"Xie","year":"2020","journal-title":"J. Catal."},{"key":"2026081412145908600_cit135","doi-asserted-by":"publisher","first-page":"4339","DOI":"10.1002\/slct.201900696","article-title":"CoFe2O4@SiO2@Co\u00ad(III) salen complex: A magnetically\nrecyclable heterogeneous catalyst for the synthesis of quinoline derivatives\nin water","volume":"4","author":"Hemmat","year":"2019","journal-title":"ChemistrySelect"},{"key":"2026081412145908600_cit136","doi-asserted-by":"publisher","first-page":"223","DOI":"10.1016\/j.mcat.2017.11.037","volume":"445","author":"Godino-Ojer","year":"2018","journal-title":"Mol. Catal."},{"key":"2026081412145908600_cit137","doi-asserted-by":"publisher","first-page":"924","DOI":"10.1002\/pssc.201000275","article-title":"Chemical synthesis of silver nanoparticles\nfor solar cell applications","volume":"8","author":"Bonsak","year":"2011","journal-title":"Phys. Status Solid\nC"},{"key":"2026081412145908600_cit138","doi-asserted-by":"publisher","first-page":"5221","DOI":"10.3390\/ijerph10105221","article-title":"Green synthesis of silver nanoparticles,\ntheir characterization, application and antibacterial activity","volume":"10","author":"Okafor","year":"2013","journal-title":"Int. J. Environ. Res. Publ. Health."},{"key":"2026081412145908600_cit139","doi-asserted-by":"publisher","first-page":"135","DOI":"10.1016\/j.arabjc.2010.04.008","article-title":"Synthesis and applications of silver nanoparticles","volume":"3","author":"Abou El-Nour","year":"2010","journal-title":"Arabian J. Chem."},{"key":"2026081412145908600_cit140","doi-asserted-by":"publisher","first-page":"1057","DOI":"10.1021\/nl034372s","article-title":"Single silver nanoparticles as real-time\noptical sensors with zeptomole sensitivity","volume":"3","author":"McFarland","year":"2003","journal-title":"Nano Lett."},{"issue":"8","key":"2026081412145908600_cit141","doi-asserted-by":"publisher","first-page":"708","DOI":"10.2174\/1385272819666150207001154","article-title":"Silver\nnanoparticles: Synthesis,\ncharacterization and their application as a sustainable catalyst for\norganic transformations","volume":"19","author":"Bhosale","year":"2015","journal-title":"Cur. Org. Chem."},{"key":"2026081412145908600_cit142","doi-asserted-by":"publisher","DOI":"10.1016\/j.cogsc.2022.100678","article-title":"Recent advances in the application\nof nanoparticles in the selective reduction of carbon\u2013carbon\ndouble bonds","volume":"38","author":"Kusy","year":"2022","journal-title":"Cur. Opin. Green Sus. Chem."},{"key":"2026081412145908600_cit143","doi-asserted-by":"publisher","first-page":"1926","DOI":"10.1080\/00397911.2019.1610776","article-title":"Green synthesis\nof silver nanoparticles using green alga (Chlorella vulgaris) and its application for synthesis of quinolines derivatives","volume":"49","author":"Mahajan","year":"2019","journal-title":"Syn. Comm."},{"key":"2026081412145908600_cit144","doi-asserted-by":"publisher","first-page":"5395","DOI":"10.1039\/C7NJ00764G","article-title":"Novel environmentally sustainable\nsynthesis of Au-Ag@AgCl nanocomposites and their application as an\nefficient and recyclable catalyst for quinoline synthesis","volume":"41","author":"Sapkota","year":"2017","journal-title":"New J. Chem."},{"key":"2026081412145908600_cit145","doi-asserted-by":"publisher","DOI":"10.1016\/j.matchemphys.2023.128126","article-title":"Ag and Ce\nnanoparticles supported on silane-modified nitrogen-doped\nmesoporous carbon (Ag,Ce@SNC\/A1SCA) obtained through green approach\nas heterogeneous catalyst towards the synthesis of 3,4-disubstituted\nisoxazol-5\u00ad(4H)-one and polyhydroquinoline derivatives","volume":"307","author":"Sharma","year":"2023","journal-title":"Mater. Chem. Phys."},{"key":"2026081412145908600_cit146","doi-asserted-by":"publisher","first-page":"13706","DOI":"10.1039\/D2RA01587K","article-title":"Recent progress\nin the applications of silica-based nanoparticles","volume":"12","author":"Nayl","year":"2022","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit147","doi-asserted-by":"publisher","first-page":"886","DOI":"10.1038\/s41578-020-0230-0","article-title":"Synthetic\namorphous silica nanoparticles: toxicity, biomedical and environmental\nimplications","volume":"5","author":"Croissant","year":"2020","journal-title":"Nat. Rev. Mater."},{"key":"2026081412145908600_cit148","doi-asserted-by":"publisher","first-page":"1337","DOI":"10.1007\/s12633-019-00229-y","article-title":"Multifaceted\napplication of silica nanoparticles. A review","volume":"12","author":"Jeelani","year":"2020","journal-title":"Silicon."},{"key":"2026081412145908600_cit149","doi-asserted-by":"publisher","first-page":"18","DOI":"10.1186\/s40486-023-00184-9","article-title":"Silicon nanoparticles: fabrication, characterization,\napplication and perspectives","volume":"11","author":"Kim","year":"2023","journal-title":"Micro. Nano Sys.\nLett."},{"key":"2026081412145908600_cit150","doi-asserted-by":"publisher","first-page":"3291","DOI":"10.1039\/c1nr10499c","article-title":"Cellular uptake, evolution,\nand excretion of silicananoparticles in human cells","volume":"3","author":"Chu","year":"2011","journal-title":"Nanoscale"},{"key":"2026081412145908600_cit151","doi-asserted-by":"publisher","first-page":"168","DOI":"10.3109\/17435390.2010.506016","article-title":"Genotoxicity evaluation of amorphous silica nanoparticles\nof different sizes using the micronucleus and the plasmid lacZ gene\nmutation assay","volume":"5","author":"Park","year":"2011","journal-title":"Nanotox."},{"key":"2026081412145908600_cit152","doi-asserted-by":"publisher","first-page":"2625","DOI":"10.1016\/j.biomaterials.2010.12.011","article-title":"Drug permeation\nacross intestinal epithelial cells using porous silicon nanoparticles","volume":"32","author":"Bimbo","year":"2011","journal-title":"Biomat."},{"key":"2026081412145908600_cit153","doi-asserted-by":"publisher","first-page":"1813","DOI":"10.1002\/ceat.201100195","article-title":"Synthesis\nof silica nanoparticles by ultrasound-assisted sol-gel method: Optimized\nby taguchi robust design","volume":"34","author":"Edrissi","year":"2011","journal-title":"Chem. Eng. Technol."},{"key":"2026081412145908600_cit154","doi-asserted-by":"publisher","first-page":"1313","DOI":"10.1007\/s11164-022-04675-z","article-title":"Synthesis\nof multiple quinoline derivatives using novel ionic liquid-based nano-magnetic\ncatalyst (MNPs@ SiO2-Pr-AP-tribromide","volume":"48","author":"Kharazmi","year":"2022","journal-title":"Res. Chem. Intermed."},{"key":"2026081412145908600_cit155","doi-asserted-by":"publisher","first-page":"201","DOI":"10.1039\/C1CY00332A","article-title":"Silica nanoparticles\nefficiently catalyzed synthesis of quinolines and quinoxalines","volume":"2","author":"Hasaninejad","year":"2012","journal-title":"Catal. Sci. Technol."},{"key":"2026081412145908600_cit156","doi-asserted-by":"publisher","DOI":"10.1002\/aoc.3566","article-title":"ZnCl2 supported on Fe3O4@SiO2 core-shell\nnanocatalyst for thesynthesis of quinolines via Friedla\u0308nder\nsynthesis under solvent-free condition","volume":"31","author":"Soleimani","year":"2017","journal-title":"Appl.\nOrganometal. Chem."},{"key":"2026081412145908600_cit157","doi-asserted-by":"publisher","first-page":"1776","DOI":"10.1002\/slct.201803708","article-title":"Mesoporous\nMCM-41 silica supported pyridine nanoparticle: A highly efficient,\nrecyclable catalyst for expeditious synthesis of quinoline derivatives\nthrough domino approach","volume":"4","author":"Mal","year":"2019","journal-title":"ChemistrySelect"},{"issue":"1","key":"2026081412145908600_cit158","doi-asserted-by":"publisher","first-page":"13","DOI":"10.1038\/s41467-017-00016-6","article-title":"Strongly bound\nexcitons in anatase TiO2 single crystals and nanoparticles","volume":"8","author":"Baldini","year":"2017","journal-title":"Nat. Commun."},{"key":"2026081412145908600_cit159","doi-asserted-by":"publisher","first-page":"30125","DOI":"10.1039\/C8RA06517A","article-title":"Recent advances\nin syntheses, properties and applications of TiO2 nanostructures","volume":"8","author":"Ali","year":"2018","journal-title":"RSC Adv."},{"key":"2026081412145908600_cit160","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1002\/9783527825431.ch1","author":"Akakuru","year":"2020","journal-title":"TiO2Nanoparticles:\nProperties and applications"},{"key":"2026081412145908600_cit161","doi-asserted-by":"publisher","first-page":"318","DOI":"10.1016\/j.cclet.2013.02.017","article-title":"Simple route to indeno\u00ad[1,2-b]\u00adquinoline\nderivatives\nvia a coupling reaction catalyzed by TiO2 nanoparticles","volume":"24","author":"Abdolmohammadi","year":"2013","journal-title":"Chin. Chem. Lett."},{"key":"2026081412145908600_cit162","doi-asserted-by":"publisher","DOI":"10.1016\/j.mcat.2019.110501","article-title":"Versatile titanium dioxide nanoparticles prepared by surface-grown\npolymerization of polyethylenimine for photodegradation and catalytic\nC\u00ad[sbnd]C bond forming reactions","volume":"475","author":"Ortiz-Bustos","year":"2019","journal-title":"Mol. Catal."},{"key":"2026081412145908600_cit163","doi-asserted-by":"publisher","first-page":"1800","DOI":"10.1002\/chem.201102151","article-title":"New Cu-based catalysts\nsupported on TiO2 films for Ullmann S NAr-type C-O coupling\nreactions","volume":"18","author":"Benaskar","year":"2012","journal-title":"Chem. Eur. J."},{"key":"2026081412145908600_cit164","doi-asserted-by":"publisher","first-page":"1702","DOI":"10.1002\/jhet.3207","article-title":"TiO2-Nanoparticles\ncatalyzed synthesis of new trifluoromethyl-4,5-dihydro-1,2,4-oxadiazoles\nand trifluoromethyl-1,2,4-oxadiazoles","volume":"55","author":"Darehkordi","year":"2018","journal-title":"J. Heterocycl.\nChem."},{"key":"2026081412145908600_cit165","doi-asserted-by":"publisher","first-page":"178","DOI":"10.1016\/j.cdc.2018.08.001","article-title":"Titanium-based\nnanoparticles:\nA novel, facile and efficient catalytic system for one-pot synthesis\nof quinoline derivatives","volume":"17\u201318","author":"Agasar","year":"2018","journal-title":"Chem. Data Coll."},{"key":"2026081412145908600_cit166","doi-asserted-by":"publisher","DOI":"10.1016\/j.heliyon.2019.e01256","article-title":"Eco-compatible\nsonochemical\nsynthesis of 8-aryl-7,8-dihydro-[1,3]-dioxolo\u00ad[4,5-g]\u00adquinolin-6\u00ad(5H)-ones\nusing green TiO2","volume":"5","author":"Bhardwaj","year":"2019","journal-title":"Heliyon"},{"key":"2026081412145908600_cit167","doi-asserted-by":"publisher","DOI":"10.1002\/aoc.5005","article-title":"Green synthesis\nof TiO2 nanoparticles as an efficient heterogeneous catalyst\nwith high reusability for synthesis of 1,2-dihydroquinoline derivatives","volume":"33","author":"El-Remaily","year":"2019","journal-title":"Appl. Organometal Chem."},{"key":"2026081412145908600_cit168","doi-asserted-by":"publisher","first-page":"1003","DOI":"10.1016\/j.cclet.2012.06.038","article-title":"TiO2 nanoparticles as an effective catalyst\nfor the synthesis of hexahydro-2-quinolinecarboxylic acids derivatives","volume":"23","author":"Abdolmohammadi","year":"2012","journal-title":"Chin. Chem. Lett."},{"key":"2026081412145908600_cit169","doi-asserted-by":"publisher","first-page":"362","DOI":"10.5560\/znb.2013-2323","article-title":"TiO2 nanoparticles\nas an efficient catalyst for the one-pot preparation of tetrahydrobenzo\u00ad[c]\u00adacridines\nin aqueous media","volume":"68b","author":"Abdolmohammadi","year":"2013","journal-title":"Z. Naturforsch."},{"key":"2026081412145908600_cit170","doi-asserted-by":"publisher","DOI":"10.1016\/j.jlumin.2022.119608","article-title":"Exciton-plasmon coupling modulation between organic-inorganic\nhybrid\nbromide lead perovskites and aluminum nanoparticle lattices","volume":"255","author":"Zhang","year":"2023","journal-title":"J. Lumin."},{"key":"2026081412145908600_cit171","doi-asserted-by":"publisher","first-page":"2229","DOI":"10.1007\/s13738-016-0941-8","article-title":"One-pot synthesis\nof 2,4-disubstituted quinolines via three-component\nreaction of amines, aldehydes and alkynes using Al2O3 nanoparticles\/methanesulfonic acid (nano-AMA) as a new catalyst","volume":"13","author":"Sharghi","year":"2016","journal-title":"Iran Chem. Soc."},{"key":"2026081412145908600_cit172","doi-asserted-by":"publisher","first-page":"2939","DOI":"10.1016\/j.jpowsour.2009.11.005","article-title":"A novel CuO-nanotube\/SnO2\ncomposite as the anode material\nfor lithium ion batteries","volume":"195","author":"Li","year":"2010","journal-title":"J. Power Sources."},{"key":"2026081412145908600_cit173","doi-asserted-by":"publisher","first-page":"6601","DOI":"10.1016\/j.apsusc.2010.04.055","article-title":"Characterization\nof nanocrystalline\nSnO2 thin film fabricated by electrodeposition method for dye-sensitized\nsolar cell application","volume":"256","author":"El-Etre","year":"2010","journal-title":"Appl. Surf. Sci."},{"key":"2026081412145908600_cit174","doi-asserted-by":"publisher","first-page":"227","DOI":"10.1016\/S1002-0721(07)60078-7","article-title":"Grain coarsening\nbehavior of Mg-Al Alloys with mischmetal addition","volume":"25","author":"Li","year":"2007","journal-title":"J. Rare Earths."},{"key":"2026081412145908600_cit175","doi-asserted-by":"publisher","first-page":"73","DOI":"10.1016\/j.molcata.2010.05.015","article-title":"Investigation of the\ncatalytic efficiency of a new mesoporous catalyst SnO2\/WO3 towards oleic acid esterification","volume":"327","author":"Sarkar","year":"2010","journal-title":"J. Mol. Catal. A: Chem."},{"key":"2026081412145908600_cit176","doi-asserted-by":"publisher","first-page":"139","DOI":"10.2174\/1570178615666180907150307","article-title":"ZnO@SnO2 mixed metal oxide as an efficient and recoverable nanocatalyst\nfor the solvent free synthesis of Hantzsch 1,4-dihydropyridines","volume":"16","author":"Sapkal","year":"2019","journal-title":"Lett. Chem."},{"key":"2026081412145908600_cit177","doi-asserted-by":"publisher","first-page":"49","DOI":"10.1186\/2228-5326-3-49","article-title":"Synthesis\nof quinoline derivatives\nfrom the reaction of aminobenzophenones and acetylenic esters in the\npresence of SnO2 nanoparticles","volume":"3","author":"Qandalee","year":"2013","journal-title":"Int.Nano\nLett."},{"key":"2026081412145908600_cit178","doi-asserted-by":"publisher","DOI":"10.1002\/aoc.7286","article-title":"Accelerated\nsonosynthesis\nof chromeno\u00ad[4,3-b]\u00adquinoline derivatives via marine-bioinspired tin\noxide nanocatalyst","volume":"37","author":"Torfi-Zadegan","year":"2023","journal-title":"Appl. Organomet. Chem."},{"issue":"20","key":"2026081412145908600_cit179","doi-asserted-by":"publisher","first-page":"4210","DOI":"10.1039\/D2NA00367H","article-title":"Zirconia-based nanomaterials: recent\ndevelopments in\nsynthesis and applications","volume":"4","author":"Kumari","year":"2022","journal-title":"Nanoscale Adv."},{"key":"2026081412145908600_cit180","doi-asserted-by":"publisher","first-page":"112","DOI":"10.1063\/1.125673","article-title":"Stable zirconium silicate gate dielectrics\ndeposited directly on silicon","volume":"76","author":"Wilk","year":"2000","journal-title":"Appl. Phys. Lett."},{"key":"2026081412145908600_cit181","doi-asserted-by":"publisher","first-page":"664","DOI":"10.1002\/adma.200500769","article-title":"Unique properties of selectively\nformed zirconia nanostructures","volume":"18","author":"Gole","year":"2006","journal-title":"Adv. Mater."},{"key":"2026081412145908600_cit182","doi-asserted-by":"publisher","first-page":"639","DOI":"10.1016\/j.snb.2006.03.044","article-title":"Development of zirconia-based\npotentiometric\nNOx sensors for automotive and energy industries in the early 21st\ncentury: What are the prospects for sensors?","volume":"121","author":"Zhuiykov","year":"2007","journal-title":"Sens. Actuators, B"},{"key":"2026081412145908600_cit183","doi-asserted-by":"publisher","first-page":"313","DOI":"10.1016\/j.cossms.2006.02.012","article-title":"Martensitic transformation in zirconia containing ceramics\nand its applications","volume":"9","author":"Jin","year":"2005","journal-title":"Curr. Opin. Solid State\nMater. Sci."},{"key":"2026081412145908600_cit184","doi-asserted-by":"publisher","DOI":"10.1002\/mds3.10076","article-title":"Nano modified zirconia\ndental implants: Advances and the frontiers for rapid osseointegration","volume":"3","author":"Gupta","year":"2020","journal-title":"Med. Devices Sens."},{"key":"2026081412145908600_cit185","doi-asserted-by":"publisher","first-page":"B74","DOI":"10.1149\/1.2434203","article-title":"Electrochemical\nintercalation of hexafluorophosphate\nanion into various carbons for cathode of dual-carbon rechargeable\nbattery","volume":"10","author":"Sholklapper","year":"2007","journal-title":"Electrochem. Solid-State Lett."},{"issue":"8","key":"2026081412145908600_cit186","doi-asserted-by":"publisher","first-page":"971","DOI":"10.2298\/JSC141023031H","article-title":"Preparation and characterization of ZrO2-supported Fe3O4-MNPs as an effective and reusable\nsuperparamagnetic catalyst for the Friedla\u0308nder synthesis of\nquinoline derivatives","volume":"80","author":"Hejazi","year":"2015","journal-title":"J. Serb. Chem. Soc."},{"issue":"8","key":"2026081412145908600_cit187","doi-asserted-by":"publisher","first-page":"1122","DOI":"10.1139\/V09-069","article-title":"Commercial\nZrO2 as a new, efficient, and\nreusable catalyst for the one-step synthesis of quinolines in solvent-free\nconditions","volume":"87","author":"Hosseini-Sarvari","year":"2009","journal-title":"Can. J. Chem."},{"issue":"2","key":"2026081412145908600_cit188","doi-asserted-by":"publisher","first-page":"1085","DOI":"10.1021\/acs.chemrev.9b00434","article-title":"Catalysis\nwith colloidal ruthenium\nnanoparticles","volume":"120","author":"Axet","year":"2020","journal-title":"Chem. Rev."},{"key":"2026081412145908600_cit189","doi-asserted-by":"publisher","first-page":"911","DOI":"10.1016\/j.psep.2022.01.054","article-title":"An\necofriendly and reusable catalyst RuO2\/MWCNT in the green synthesis\nof sulfonyl-quinolines","volume":"159","author":"Harikrishna","year":"2022","journal-title":"Pro. Safety Envir. Prot."},{"issue":"8","key":"2026081412145908600_cit190","doi-asserted-by":"publisher","first-page":"2198","DOI":"10.1002\/cctc.201902311","article-title":"Pr2O3 supported\nnano-layered\nruthenium catalyzed acceptorless dehydrogenative synthesis of 2-substituted\nquinolines and 1,8-naphthyridines from 2-aminoaryl alcohols and ketones","volume":"12","author":"Chaudhari","year":"2020","journal-title":"ChemCatChem."},{"key":"2026081412145908600_cit191","doi-asserted-by":"publisher","first-page":"3018","DOI":"10.1002\/slct.201602069","article-title":"Supramolecular\nensemble\nof tetraphenylcyclopentadienone derivative and HgO nanoparticles:\nA one-pot approach for the synthesis of quinoline and quinolone derivatives","volume":"2","author":"Kataria","year":"2017","journal-title":"Chemistry Select"},{"key":"2026081412145908600_cit192","doi-asserted-by":"publisher","DOI":"10.1016\/j.poly.2020.114459","article-title":"A highly\neffective synthesis of pyrimido\u00ad[4,5-b]\u00adquinoline-tetraones using H3PW12O40\/chitosan\/NiCo2O4 as a novel magnetic nanocomposite","volume":"182","author":"Safari","year":"2020","journal-title":"Polyhedron"},{"key":"2026081412145908600_cit193","doi-asserted-by":"publisher","first-page":"338","DOI":"10.1007\/s10562-015-1652-y","article-title":"Nano KF\/Clinoptilolite:\nAn effective heterogeneous base nanocatalyst for synthesis of substituted\nquinolines in water","volume":"146","author":"Sajjadi-Ghotbabadi","year":"2016","journal-title":"Catal. Lett."},{"key":"2026081412145908600_cit194","doi-asserted-by":"publisher","first-page":"29","DOI":"10.1016\/j.ijbiomac.2019.12.059","article-title":"Preparation of a novel magnetic bionanocomposite\nbased\non factionalized chitosan by creatine and its application in the synthesis\nof polyhydroquinoline, 1,4-dyhdropyridine and 1,8-dioxodecahydroacridine\nderivatives","volume":"144","author":"Asgharnasl","year":"2020","journal-title":"Inter. J. Bio. Macromol."}],"container-title":["ACS Omega"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acsomega.4c07011","content-type":"application\/pdf","content-version":"vor","intended-application":"unspecified"},{"URL":"https:\/\/pubs.acs.org\/acsodf\/article-pdf\/9\/42\/42630\/4115358\/ao4c07011.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/pubs.acs.org\/acsodf\/article-pdf\/9\/42\/42630\/4115358\/ao4c07011.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T16:15:11Z","timestamp":1786724111000},"score":1,"resource":{"primary":{"URL":"https:\/\/pubs.acs.org\/acsodf\/article\/9\/42\/42630\/409751\/Quinoline-Synthesis-Nanocatalyzed-Green-Protocols"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,10,14]]},"references-count":208,"journal-issue":{"issue":"42","published-online":{"date-parts":[[2024,10,14]]},"published-print":{"date-parts":[[2024,10,22]]}},"URL":"https:\/\/doi.org\/10.1021\/acsomega.4c07011","relation":{},"ISSN":["2470-1343"],"issn-type":[{"value":"2470-1343","type":"electronic"}],"subject":[],"published":{"date-parts":[[2024,10,14]]}}}