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<ArticleSet>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Application of dimeric ortho-palladated complex of 2-methoxyphenethylamine in the Heck coupling reaction</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Application of dimeric ortho-palladated complex of 2-methoxyphenethylamine in the Heck coupling reaction</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Abdol</FirstName>
				<LastName>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>Fatemeh</FirstName>
				<LastName>Abrishami</LastName>
				<Affiliation>Department of Chemistry and Chemical Engineering, Malek-Ashtar University of Technology, Tehran, 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 application of the [Pd{C6H3(CH2CH2NH2)-4-OMe-5-κ2-C,N}(μ-Br)]2 complex of 2-methoxyphenethylamine in the Heck coupling reaction was considered under both conventional and microwave irradiation conditions, and their results were compared. This complex is an efficient, stable and non-sensitive to air and moisture catalyst for the vinylation of substituted aryl halides with different electronic properties. The cross-coupled products were produced in good to excellent yields using a catalytic amount of this complex in N-methyl-2-pyrrolidone (NMP) at 130 °C. In comparison to conventional heating conditions, the reactions under microwave irradiation gave higher yields in shorter reaction times.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Microwave irradiation</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Heck reaction</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">2-Methoxyphenethylamine</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Cyclopalladated complex</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Catalyst</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>NanoZnO as an efficient &amp; reusable catalyst for the preparation of 1,4-DHPs via Hantzsch reaction</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>NanoZnO as an efficient &amp; reusable catalyst for the preparation of 1,4-DHPs via Hantzsch reaction</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Fatemeh</FirstName>
				<LastName>Tamaddon</LastName>
				<Affiliation>Department of Chemistry, Faculty of Science, Yazd University, Yazd 89195-741, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Somayeh</FirstName>
				<LastName>Moradi</LastName>
				<Affiliation>Department of Chemistry, Faculty of Science, Yazd University, Yazd 89195-741, 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>Easily prepared nanoZnO was found to be as an efficient catalyst in the synthesis of 1,4-DHPs via four-component reaction of 1,3-dicarbonyls, aldehydes and ammonium carbonate in water at 60 °C. The prepared nanoZnO was characterized by XRD and FT-IR analysis, while the determined specific surface area of nano catalyst by BET method was 33 m2/g.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">NanoZnO</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Four-component reaction</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">DHPs</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Ammonium carbonate</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Triethylamine-bonded sulfonic acid {[Et3N-SO3H]Cl} as an efficient and homogeneous catalyst for the synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Triethylamine-bonded sulfonic acid {[Et3N-SO3H]Cl} as an efficient and homogeneous catalyst for the synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Abdolkarim</FirstName>
				<LastName>Zare</LastName>
				<Affiliation>Department of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, Iran</Affiliation>
				<Identifier Source="ORCID">0000-0002-8210-3155</Identifier>
			</Author>
            			<Author>
                				<FirstName>Roghayyeh</FirstName>
				<LastName>Khanivar</LastName>
				<Affiliation>Department of Chemistry, Payame Noor University, PO BOX 19395-4697, Tehran, Iran</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Maria</FirstName>
				<LastName>Merajoddin</LastName>
				<Affiliation>Department of Chemistry, Payame Noor University, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Masoud</FirstName>
				<LastName>Kazem-Rostami</LastName>
				<Affiliation>Young Researchers Club, Takestan Branch, Islamic Azad University, Takestan, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Mohammad</FirstName>
				<LastName>Mahdi Ahmad-Zadeh</LastName>
				<Affiliation>Department of Chemistry, Payame Noor University, PO BOX 19395-4697, Tehran, Iran</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Ahmad</FirstName>
				<LastName>Reza Moosavi-Zare</LastName>
				<Affiliation>Department of Chemistry, Sayyed Jamaleddin Asadabadi University, Asadabad, 6541861841, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Alireza</FirstName>
				<LastName>Hasaninejad</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>Brønsted acidic ionic liquid triethylamine-bonded sulfonic acid {[Et3N-SO3H]Cl} efficiently catalyzes the one-pot multi-component condensation of 2-naphthol with arylaldehydes and dimedone (5,5-dimethylcyclohexane-1,3-dione) under solvent-free conditions to afford 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones in high yields and relatively short reaction times.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">2-Naphthol</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Bronsted acidic ionic liquid</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Triethylamine-bonded sulfonic acid {[Et3N-SO3H]Cl}</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">12-Aryl-8</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">9</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">10. 12-tetrahydrobenzo[a]xanthen-11-one</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Introduction of two efficient catalysts for the synthesis of 1,8-dioxo-octahydroxanthene derivatives in the absence of solvent</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Introduction of two efficient catalysts for the synthesis of 1,8-dioxo-octahydroxanthene derivatives in the absence of solvent</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>Gholam</FirstName>
				<LastName>Hossein Imanzadeh</LastName>
				<Affiliation>Department of Chemistry, College of Science, University of Mohaghegh Ardabili, Ardabil, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Masoumeh</FirstName>
				<LastName>Abedini</LastName>
				<Affiliation>Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Maryam</FirstName>
				<LastName>Akberi Dokhte-Ghaziani</LastName>
				<Affiliation>Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Mohaddeshes</FirstName>
				<LastName>Safarpoor Langroodi</LastName>
				<Affiliation>Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Parisa</FirstName>
				<LastName>Ghods Ghasemabadi</LastName>
				<Affiliation>Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.
Department of Chemistry, College of Science, University of Mohaghegh Ardabili, Ardabil, 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>1,3-Dibromo-5,5-dimethylhydantoin (DBH) and benzyltriphenylphosphoniumtribromide (BTPTB) were used as efficient catalysts for the promotion of the synthesis of 1,8-dioxo-octahydroxanthene derivatives (DOXOs) via a one-pot three component condensation of aldehydes and cyclic 1,3-dicarbonyl compounds in the absence of solvent.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">3-dicarbonyl compounds. 3-Dibromo-5</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">5-dimethylhydantoin</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Aldehydes</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">8-Dioxo-octahydroxanthenes</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Cyclic 1</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Magnetic Fe3O4 nanoparticles as a highly efficient catalyst for the synthesis of imidazoles under ultrasound irradiation</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Magnetic Fe3O4 nanoparticles as a highly efficient catalyst for the synthesis of imidazoles under ultrasound irradiation</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Javad</FirstName>
				<LastName>Safari</LastName>
				<Affiliation>Laboratory of Organic Compound Research, Department of Organic Chemistry, College of Chemistry, University of Kashan, P.O. Box: 87317-51167 Kashan, I.R. Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Zohre</FirstName>
				<LastName>Zarnegar</LastName>
				<Affiliation>Laboratory of Organic Compound Research, Department of Organic Chemistry, College of Chemistry, University of Kashan, P.O. Box: 87317-51167, Kashan, 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>To be fairly general and catalyst is easily separated by magnetic devices and can be reused without any apparent loss of activity for the reaction. Fe3O4 nanoparticles were prepared by chemical coprecipitation method and was found to be a mild and effective catalyst for the efficient, one-pot, three-component synthesis of 2,4,5-trisubstituted imidazoles at room temperature under ultrasound irradiation. The high yields of products and short reaction time were attributed to the nanosize of about 20 nm in which the catalyst could act as a nanoreactor. This methodology is found.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Heterogeneous catalyst</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Fe3O4 nanoparticles</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">imidazole</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">ultrasound irradiation</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Bi(NO3)3.5H2O: An efficient acidic reagent for synthesis of azo dyes at room temperature</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Bi(NO3)3.5H2O: An efficient acidic reagent for synthesis of azo dyes at room temperature</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Bi</FirstName>
				<LastName>Bi Fatemeh Mirjalili</LastName>
				<Affiliation>Department of Chemistry, College of Science, Yazd University, Yazd, P.O. Box 89195-741, Iran</Affiliation>
				<Identifier Source="ORCID">0000-0002-6588-4041</Identifier>
			</Author>
            			<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>Naimeh</FirstName>
				<LastName>Salehi</LastName>
				<Affiliation>Department of Chemistry, College of Science, Yazd University, Yazd, P.O. Box 89195-741, 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 one-pot method has been developed for the synthesis of azo dyes via sequential diazotization–diazo coupling of aromatic amines with coupling agents at room temperature in the presence of Bi(NO3)3. 5H2O. Short reaction times, high yields, a clean process, simple methodology, easy work-up and green ‎conditions are advantages of this protocol.‎</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">One-pot synthesis</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Azo dye.</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Bi(NO3)3.SiO2</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Stable diazonium salts</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Photocatalytic efficiency of CuFe2O4 by supporting on clinoptilolite in the decolorization of acid red 206 aqueous solutions</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Photocatalytic efficiency of CuFe2O4 by supporting on clinoptilolite in the decolorization of acid red 206 aqueous solutions</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Azar</FirstName>
				<LastName>Bagheri Ghomi</LastName>
				<Affiliation>Department of Chemistry, Center Tehran Branch, Islamic Azad University, Tehran, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Vahid</FirstName>
				<LastName>Ashayeri</LastName>
				<Affiliation>Department of Chemistry, Center Tehran Branch, Islamic Azad University, Tehran, 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 paper CuFe2O4, nanocrystalline powders were prepared. Also, the supported Cu ferrite was obtained by impregnation of the supports with Cu and Fe nitrates solutions, for calcination temperature 450 ºC. The samples were characterized by X-ray powder diffraction (XRD) and Fourier transform-infrared spectroscopy (FT-IR). Photocatalytic degradation of acid red 206 in water was studied. CuFe2O4 was supported on Clinoptilolite using solid-state dispersion (SSD) method. The results show that the CuFe2O4/zeoliteis an active photocatalyst. The maximum effect of photodegradation was observed at 10 wt. %CuFe2O4, 90 %wt. Clinoptilolite. A first order reaction with k = 0.123 min-1 was observed. The effects of some parameters such as pH, amount of photocatalyst, initial concentration of dye were examined.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Photodegradation</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Photocatalysts.</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">CuFe2O4/Zeolites</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Acid Red 206</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Clinoptilolite.</Param>
			</Object>
					</ObjectList>
	</Article>
		<Article>
		<Journal>
			<PublisherName>Iranian Journal of Catalysis (IJC)</PublisherName>
			<JournalTitle>Urea-hydrogen peroxide/silica phosphoric acid-catalyzed oxidation- condensation Tandem reaction: One-pot synthesis of 2-substituted benzimidazoles from alcohols</JournalTitle>
			<Issn></Issn>
			<Volume>Volume 2 (2012)</Volume>
			<Issue>Issue 3, September 2012</Issue>
			<PubDate PubStatus="epublish">
                <Year>2024</Year>
                <Month>02</Month>
                <Day>03</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Urea-hydrogen peroxide/silica phosphoric acid-catalyzed oxidation- condensation Tandem reaction: One-pot synthesis of 2-substituted benzimidazoles from alcohols</ArticleTitle>
		<VernacularTitle></VernacularTitle>
		<FirstPage></FirstPage>
		<LastPage></LastPage>
		<ELocationID EIdType="doi"></ELocationID>
		<Language>EN</Language>
		<AuthorList>
            			<Author>
                				<FirstName>Ahmad</FirstName>
				<LastName>Reza Momeni</LastName>
				<Affiliation>Department of Chemistry, Faculty of Science, Shahrekord University, Shahrekord, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Heshmat</FirstName>
				<LastName>Allah Samimi</LastName>
				<Affiliation>Faculty of Sciences, Shahrekord University, 115-381, Shahrekord, Iran.</Affiliation>
				<Identifier Source="ORCID"></Identifier>
			</Author>
            			<Author>
                				<FirstName>Reyhaneh</FirstName>
				<LastName>Jahanian</LastName>
				<Affiliation>Faculty of Sciences, Shahrekord University, 115-381, Shahrekord, 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 one-pot oxidation/condensation tandem process has been developed for the synthesis of 2-substituted benzimidazole derivatives from benzylic alcohols and 1,2-phenylenediamine with use of urea-hydrogen peroxide/silica phosphoric acid  as a bifunctional catalyst. This method provides a rapid and efficient access to 2-substituted benzimidazoles.</Abstract>
		<ObjectList>
            			<Object Type="keyword">
				<Param Name="value">Silica phosphoric acid</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Benzimidazoles</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Alcohols</Param>
			</Object>
						<Object Type="keyword">
				<Param Name="value">Urea-hydrogen peroxide</Param>
			</Object>
					</ObjectList>
	</Article>
	</ArticleSet>
