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            <name>Title</name>
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    <name>Article</name>
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          <name>Title</name>
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              <text>Environmentally conscious synthesis of novel pyrano[2,3-d]pyrimidines via ternary deep eutectic solvents</text>
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          <name>Subject</name>
          <description>The topic of the resource</description>
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              <text>Catalytic solvent; Deep eutectic solvents; Four-component reaction; Open-flask; Pyrano[2,3-d]pyrimidine; Sustainable synthesis</text>
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          <name>Description</name>
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              <text>Pyrano[2,3-d]pyrimidine and its analogues have gained considerable courtesy because of their diverse biological functions and wide-ranging applications, from pharmaceutical agents to essential natural pigments. However, synthesising pyrano[2,3-d]pyrimidine with multiple reactants is challenging and requires advanced green chemistry solutions. This study investigates the generation of thirteen new pyrano[2,3-d]pyrimidine analogues through a single-step, open-flask, multicomponent reaction (MCR) strategy involving aldehydes, phenylhydrazine, ethyl acetoacetate, and barbituric acid via deep eutectic solvents (DES). These DESs serve as environmentally friendly alternatives to traditional solvents. A ternary deep eutectic solvent (TDES) was evaluated for its catalytic solvent activity among ten different formulations. TDES-7 (5 mL) demonstrated the best performance, achieving 95 % product formation within 30 min at room temperature. Its remarkable catalytic activity and ability to produce high yields across multiple reaction cycles make it a standout choice for this application. The collaboration between MCR and TDES underscores an important blend of two significant green aspects, demonstrating their potential to achieve a green and productive sustainable synthesis method with an noble E-factor of 0.1236.  2024 Elsevier B.V.</text>
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          <name>Creator</name>
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              <text>Kumar S.L.; Tabassum S.; Govindaraju S.</text>
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          <name>Source</name>
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              <text>Journal of Molecular Liquids, Vol-417</text>
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          <name>Publisher</name>
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              <text>Elsevier B.V.</text>
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          <name>Date</name>
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              <text>2025-01-01</text>
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          <name>Identifier</name>
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              <text>&lt;a href="https://doi.org/10.1016/j.molliq.2024.126651" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1016/j.molliq.2024.126651&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85211185034&amp;amp;doi=10.1016%2Fj.molliq.2024.126651&amp;amp;partnerID=40&amp;amp;md5=06264166a44074bfd54945bd61b38d7e" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85211185034&amp;amp;doi=10.1016%2fj.molliq.2024.126651&amp;amp;partnerID=40&amp;amp;md5=06264166a44074bfd54945bd61b38d7e&lt;/a&gt;</text>
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          <name>Rights</name>
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              <text>Restricted Access</text>
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          <description>A related resource</description>
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              <text>ISSN: 1677322; CODEN: JMLID</text>
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          <name>Format</name>
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              <text>Online</text>
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          <name>Language</name>
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              <text>English</text>
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              <text>Kumar S.L., Department of Chemistry, Christ University, Bengaluru, 560029, India; Tabassum S., Department of Chemistry, Surana College, Bengaluru, 560074, India; Govindaraju S., Department of Sciences and Humanities, Christ University, Bengaluru, 560074, India</text>
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