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<ArticleSet>
<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Iranian Journal of Catalysis</JournalTitle>
<Issn>2345-4865</Issn>
<Volume>2</Volume>
<Issue>4</Issue>
<PubDate PubStatus="epublish">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</Journal>
<ArticleTitle>A fast, simple and convenient procedure for the synthesis of fused pyrimidinone derivatives by using [Hmim][HSO4] as a green, efficient and reusable catalyst under 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>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 R.</FirstName>
<LastName>Hajipour</LastName>
<Affiliation>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>In the present of methylimidazolium hydrogen sulfate, the synthesis of arylidene heterobicyclic pyrimidinones is studied by condensation of aromatic aldehyde, cyclopentanone, and urea or thiourea. Using solvent-free conditions, non-toxic and inexpensive materials, simple and clean work-up, short reaction times and good yields of the products are the advantages of this method.</Abstract>
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<Object Type="keyword">
<Param Name="value">Biginelli-type reaction</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Bronsted acidic ionic liquid</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Methylimidazolium hydrogen sulfate</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Pyrimidinone</Param>
</Object>
</ObjectList>
</Article>
</ArticleSet>