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<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Iranian Journal of Catalysis</JournalTitle>
<Issn>2345-4865</Issn>
<Volume>6</Volume>
<Issue>4</Issue>
<PubDate PubStatus="epublish">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</Journal>
<ArticleTitle>Mesolite catalyzed one pot synthesis of quinoline-3-carbonitrile derivatives</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage></FirstPage>
<LastPage></LastPage>
<ELocationID EIdType="doi"></ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Ganesh T.</FirstName>
<LastName>Pawar</LastName>
<Affiliation>Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Rameshwar R.</FirstName>
<LastName>Magar</LastName>
<Affiliation>Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Machhindra K.</FirstName>
<LastName>Lande</LastName>
<Affiliation>Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India.</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>Natural mesolite type zeolite was collected, modified by sulfuric acid treatment and characterized by using Powder-X ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR).Temperature programmed ammonia desorption (NH3-TPD), Brunauer-Emmer-Teller (BET) surface area analysis.  Modified dealuminated mesolite shows an efficient catalytic activity for the one-pot synthesis of quinoline-3-carbonitrile derivatives, via three-component cyclocondensation of benzaldehyde, malononitrile and aniline.  The present method offers several advantages over the reported methods like simple and inexpensive modification of the catalyst, mild reaction conditions and easy separation of the catalyst, simple work-up procedures, non-chromatographic separation and purification of desired product, excellent yield and reusability of the catalyst.</Abstract>
<ObjectList>
<Object Type="keyword">
<Param Name="value">aniline</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Benzaldehyde</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Malononitrile</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Mesolite</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Modification of natural zeolite</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Quinoline-3-carbonitile</Param>
</Object>
</ObjectList>
</Article>
</ArticleSet>