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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Journal of Nanostructure in Chemistry</JournalTitle>
<Issn>2193-8865</Issn>
<Volume>13</Volume>
<Issue>4 (August 2023)</Issue>
<PubDate PubStatus="epublish">
<Year>2021</Year>
<Month>10</Month>
<Day>14</Day>
</PubDate>
</Journal>
<ArticleTitle>Synthesis of benzothiazole and benzimidazole derivatives via an eco-friendly method using piperazine immobilized on nano-ZnO-sulfuric acid as a powerful catalyst</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage></FirstPage>
<LastPage></LastPage>
<ELocationID EIdType="doi">10.1007/s40097-021-00450-5</ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Maryam</FirstName>
<LastName>Mousapour</LastName>
<Affiliation>Department of Chemistry, College of Sciences, University of Guilan, Rasht, 41335-19141, IR</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Farhad</FirstName>
<LastName>Shirini</LastName>
<Affiliation>Department of Chemistry, College of Sciences, University of Guilan, Rasht, 41335-19141, IR</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
</AuthorList>
<PublicationType>Journal Article</PublicationType>
<History>
<PubDate PubStatus="received">
<Year>2021</Year>
<Month>10</Month>
<Day>14</Day>
</PubDate>
</History>
<Abstract>Abstract
In this research, the synthesis of piperazine immobilized on nano-ZnO-sulfuric acid (PINZS) as a new piperazine-based nano-reagent is reported. After identification of PINZS using different techniques including XRD (X-ray powder diffraction), TGA (thermogravimetric analysis), FT-IR (Fourier transform infrared spectroscopy), FESEM (field emission scanning electron microscopy), and EDX (energy-dispersive X-ray) analysis, this reagent is efficiently used for the synthesis of 1-(benzothiazolylamino) phenylmethyl-2-naphthols and pyrimido[1, 2-a]benzimidazoles via a domino Knoevenagel/Michael sequence which identified acceptable reaction times (7–45 min.), great yields (up to 98%) and ease of the preparation, separation, and recovery of PINZS (for three times) as the most important features of this protocol.
Graphic abstract
Use of PINZS in the synthesis of some important heterocycles.
</Abstract>
<ObjectList>
<Object Type="keyword">
<Param Name="value">ZnO NPs</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Piperazine</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Immobilized ionic liquids</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Multi-component reactions</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Pyrimido[1,2-a]benzimidazole</Param>
</Object>
<Object Type="keyword">
<Param Name="value">1-(Benzothiazolylamino) phenylmethyl-2-naphthol</Param>
</Object>
</ObjectList>
</Article>
</ArticleSet>