<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Synthesis, characterization and photocatalytic activity of CeO2-SBA-15</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Synthesis, characterization and photocatalytic activity of CeO2-SBA-15</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Hamid</FirstName>
				<LastName>Reza Pouretedal</LastName>
				<Affiliation>Department of Applied Chemistry, Maleke-ashtar University of Technology, Shahin-shahr, Esfahan, Iran</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Sara</FirstName>
				<LastName>Basati</LastName>
				<Affiliation>Department of Chemistry, Shahreza Branch, Islamic Azad University, Shahreza, 86145-311, Iran</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>Mesoporous photocatalysts of CeO2/SBA-15 are prepared by two methods of direct synthesis as solvent-usage and solvent-free methods. In solvent-usage method, CeO2/SBA-15 is synthesized in acidic media. While, in solvent-free method, CeO2/SBA-15, has been prepared through the novel path of directly grind cerium salt into the as-prepared samples of SBA-15 occluded with template. This method enables a large amount of cerium to be highly dispersed in the channels of mesoporous silica, also saves time and energy. The resulting composites exhibit photocatalytic activity, and the dispersed CeO2 in SBA-15 illustrates a photodegradation of Congo red (CR) in aqueous solution. X-ray powder diffraction, N2 adsorption-desorption and FT-IR spectroscopy are used to characterize the prepared materials.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Photocatalyst</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">SBA-15</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">nanoparticles</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">CeO2</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Congo red (CR)</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Synthesis of 1,3,5-tri-substituted pyrazoles promoted by P2O5.SiO2</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Synthesis of 1,3,5-tri-substituted pyrazoles promoted by P2O5.SiO2</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Abdolhamid</FirstName>
				<LastName>Bamoniri</LastName>
				<Affiliation>Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan, Iran</Affiliation>
				<Identifier Source="ORCID">0000-0002-8911-2433</Identifier>
			</Author>
            			<Author>
                				<FirstName>BiBi</FirstName>
				<LastName>Fatemeh Mirjalili</LastName>
				<Affiliation>Department of Chemistry, College of Science, Yazd University, P. O. Box 89195-741, Yazd. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Abbas</FirstName>
				<LastName>Ali Jafari</LastName>
				<Affiliation>Department of Chemistry, College of Science, Yazd University, P.O.Box 89195-741, Yazd, I.R.Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Fatemeh</FirstName>
				<LastName>Abasaltian</LastName>
				<Affiliation>Department of Chemistry, College of Science, Yazd University, P.O.Box 89195-741, Yazd, I.R.Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>Silica supported phosphorus pentoxide (P2O5·SiO2) is an efficient catalyst for synthesis of 1,3,5-substituted pyrazoles via the condensation of 1,3-diketones and hydrazines. Simplicity of procedure, mild condition, being solvent-free, high yields, and easy workup are some advantages of this protocol.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">5-tri-substituted pyrazoles</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">3-diketones. Hydrazines</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Solvent-free</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">P2O5.SiO2</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>1,3-Dichloro-5,5-dimethylhydantoin: an efficient catalyst for the solvent free synthesis of 1,8-dioxo-octahydro-xanthenes</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>1,3-Dichloro-5,5-dimethylhydantoin: an efficient catalyst for the solvent free synthesis of 1,8-dioxo-octahydro-xanthenes</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Farhad</FirstName>
				<LastName>Shirini</LastName>
				<Affiliation>Department of Chemistry, College of Science, University of Guilan, Rasht, Iran</Affiliation>
				<Identifier Source="ORCID">0000-0002-7204-5000</Identifier>
			</Author>
            			<Author>
                				<FirstName>Kurosh</FirstName>
				<LastName>Rad-Moghadam</LastName>
				<Affiliation>Chemistry Department, University of Guilan, P.O. Box 41335-19141, Rasht, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Tahereh</FirstName>
				<LastName>Naghdi</LastName>
				<Affiliation>Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>This paper describes the applicability of 1,3-dichloro-5,5-dimethylhydantoin, as a cheap, stable and commercially available catalyst, in the promotion of the synthesis of 1,8-dioxo-octahydro-xanthenes (DOXOs) via the one-pot condensation of aldehydes and cyclic 1,3-dicarbonyl compounds. This novel synthetic method has the advantages of high yields, short reaction times, low cost and availability of the catalyst, solvent-free reaction conditions, simplicity and easy work-up compared to the conventional methods reported in the literature.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Aldehydes</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">8-Dioxo-octahydro-xanthenes</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">3-Dichloro-5</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">5-dimethylhydantoin. Cyclic 1</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">3-dicarbonyl compounds</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Brønsted acidic ionic liquid as a metal free catalyst for the one-pot synthesis of α-aminonitriles under mild and solvent-free conditions</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Brønsted acidic ionic liquid as a metal free catalyst for the one-pot synthesis of α-aminonitriles under mild and solvent-free conditions</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Leila</FirstName>
				<LastName>Khazdooz</LastName>
				<Affiliation>Department of Science, Isfahan (Khorasgan) Branch, Islamic Azad University, Isfahan 81595-158, Iran

Laser and Biophotonics in Biotechnologies Research Center, Isfahan (Khorasgan) Branch, Islamic Azad University, Isfahan 81595-158, Iran</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Amin</FirstName>
				<LastName>Zarei</LastName>
				<Affiliation>Department of Science, Fasa Branch, Islamic Azad University, PO Box No. 364, Fasa 7461713591, Fars, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Abdol</FirstName>
				<LastName>R. Hajipour</LastName>
				<Affiliation>Pharmaceutical Research Laboratory, Department of Chemistry, Isfahan University of Technology, Isfahan 84156, Iran.
Department of Pharmacology, University of Wisconsin, Medical School, 1300 University Avenue, Madison, 53706-1532, WI, USA.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Nafisehsadat</FirstName>
				<LastName>Sheikhan</LastName>
				<Affiliation>Department of Chemistry, Faculty of Sciences, Najafabad Branch, Islamic Azad University, Najafabad, Esfahan, P.O. Box 517, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>An efficient, mild and environmentally friendly method was developed for the Strecker reaction to synthesize α-aminonitriles in the presence of methyl imidazolium hydrogen sulfate ([Hmim][HSO4]) as an efficient catalyst. These syntheses were performed via a one-pot three-component condensation of aldehydes (or ketones), amines, and trimethylsilyl cyanide under mild and solvent free conditions.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">α-Amino nitriles</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Strecker</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Methyl imidazolium hydrogen sulfate</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Solvent-free conditions</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Synthesis of 4,4′-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Synthesis of 4,4′-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Shekoofeh</FirstName>
				<LastName>Tayebi</LastName>
				<Affiliation>Young Researchers Club, Gachsaran Branch, Islamic Azad University, Gachsaran, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Khodabakhsh</FirstName>
				<LastName>Niknam</LastName>
				<Affiliation>Department of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr 75169, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>The one-pot, multi-component synthesis of 4,4′-(arylmethylene)bis(1H-pyrazol-5-ols) by tandem Knoevenagel-Michael reaction of phenylhydrazine, ethyl acetoacetate and aldehydes in the presence of silica-bonded N-propylpiperazine sulfamic acid (SBPPSA) as a recyclable solid acid catalyst was reported. SBPPSA showed much the same efficiency when used in consecutive reaction runs.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Catalyst</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Aldehydes</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Silica-bonded N-propylpiperazine sulfamic acid</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">4</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">4′-(Arylmethylene)bis(1H-pyrazol-5-ols). Multi-component reactions</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Kinetic investigation of photocatalytic degradation of dimethyldisulfide by zeolite A containing nano CdS</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Kinetic investigation of photocatalytic degradation of dimethyldisulfide by zeolite A containing nano CdS</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Alireza</FirstName>
				<LastName>Nezamzadeh-Ejhieh</LastName>
				<Affiliation>Department of Chemistry, Shahreza Branch, Islamic Azad University, P.O. Box 311-86145, Shahreza, Isfahan, Iran</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Zohreh</FirstName>
				<LastName>Banan</LastName>
				<Affiliation>Department of Chemistry, Shahreza Branch, Islamic Azad University, P.O. Box 311-86145, Shahreza, Isfahan, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>In this research, zeolite A was synthesized from waste porcelain and CdS nano-particles were doped in zeolite framework by a precipitation after an ion exchanging process. All raw and modified samples were characterized by FT-IR, XRD and SEM methods. Primary experiments showed that the good efficiency of loaded nano CdS onto the zeolite A for photodecomposition of dimethyldisulfide (DMDS) under UV irradiation. Hence the effect of some experimental parameters on the kinetics of the photodegradation experiments was studied and the optimal conditions were found as: pH 3, 3 g L–1 of the catalyst and 8 ppm of DMDS concentration. UV-Vis spectrophotometric measurements were performed to determine the degradation extent. The degradation process obeyed first-order kinetics.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Zeolite A</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Dimethydisulfide</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">CdS nanoparticles</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Heterogeneous catalysis</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>A new, green and recyclable poly(4-vinylpyridine)-supported copper iodide nanoparticles catalyst for the synthesis of aryl-14H-dibenzo [a-o] xanthenes</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>A new, green and recyclable poly(4-vinylpyridine)-supported copper iodide nanoparticles catalyst for the synthesis of aryl-14H-dibenzo [a-o] xanthenes</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Jalal</FirstName>
				<LastName>Albadi</LastName>
				<Affiliation>Department of Chemistry, Faculty of Science, Shahrekord University, Shahrekord, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Nasir</FirstName>
				<LastName>Iravani</LastName>
				<Affiliation>Department of Chemistry, Faculty of Science, Gachsaran Branch, Islamic Azad University, Gachsaran, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Moloud</FirstName>
				<LastName>Khoshakhlagh</LastName>
				<Affiliation>Department of Chemistry, Gachsaran Branch, Islamic Azad University, Gachsaran, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>Poly(4-vinylpyridine)-supported copper iodide nanoparticles is reported as a new, green and recyclable catalyst for the synthesis of aryl-14H-dibenzo [a-o] xanthenes under solvent-free conditions. This catalyst can be recovered by simple filtration and recycled up to 8 consecutive runs without any loss of their efficiency.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">nanoparticles</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Poly(4-vinylpyridine)-Supported</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">β-naphthol</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">aryl-14H-dibenzo [a-o] xanthenes</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Copper catalysis. Solvent-free conditions</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Sulfonated Porous Carbon (SPC): An efficient and recyclable solid acid catalyst for one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones under solvent-free conditions</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 2, June 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Sulfonated Porous Carbon (SPC): An efficient and recyclable solid acid catalyst for one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones under solvent-free conditions</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Arash</FirstName>
				<LastName>Shokrolahi</LastName>
				<Affiliation>Chemistry Department, Malek-ashtar University of Technology, Shahin Shahr, P.O.Box 83145-115, I. R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Abbas</FirstName>
				<LastName>Zali</LastName>
				<Affiliation>Chemistry Department, Malek-ashtar University of Technology, Shahin Shahr, P.O.Box 83145-115, I. R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Mohammad</FirstName>
				<LastName>Ali Zarei</LastName>
				<Affiliation>Chemistry Department Faculty of Materials, Malek-ashtar University of Technology, Tehran, I.R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Karim</FirstName>
				<LastName>Esmaeilpour</LastName>
				<Affiliation>Chemistry Department, Malek-ashtar University of Technology, Shahin-shahr, P.O.Box 83145-115, I. R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            		</AuthorList>
		<PublicationType>Journal Article</PublicationType>
		<History>
			<PubDate PubStatus="received">
				<Year>2024</Year>
				<Month>02</Month>
				<Day>03</Day>
			</PubDate>
		</History>
		<Abstract>A simple and efficient procedure has been developed for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones derivatives under solvent-free conditions. This method uses the condensation of isatoic anhydride, aldehydes, and amines in the presence of a catalytic amount Sulfonated Porous Carbon (SPC). One of the important advantages of the new method is that the SPC could be recycled and reused.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Solid acid</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Sulfonated Porous Carbon</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Heterogeneous catalysis</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">3-Dihydroquinazolin-4(1H)-ones</Param>
			</Object>
					</ObjectList>
	</Article>
	</ArticleSet>
