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                <text>Faculty Publications</text>
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    <name>Article</name>
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          <name>Creator</name>
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              <text>Tabassum, Sumaiya; Govindaraju, Santhosh</text>
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          <name>Title</name>
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              <text>White LED Light-Mediated Eosin Y-Photocatalyzed One-Pot Synthesis of Novel 1,2,4-Triazol-3-Amines By Sequential Addition</text>
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              <text>01-01-2025</text>
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              <text>Topics in Catalysis;Volume;68;Issue;13;pp.1523-1533</text>
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              <text>&lt;a href="https://doi.org/10.1007/s11244-022-01590-w" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1007/s11244-022-01590-w&lt;/a&gt; &lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/pages/publications/85124333009?origin=resultslist" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/pages/publications/85124333009?origin=resultslist&lt;/a&gt;</text>
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              <text>Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India</text>
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              <text>Abstract: A facile and proficient, eco-friendly multicomponent synthesis of 12 novel biologically essential 1,2,4-triazol-3-amines via the sequential addition of substituted phenacyl bromide, aromatic aldehyde, hydrazinecarbothioamide, and urea under white LED with eosin Y as a photocatalyst has been developed. The intrinsic advantages are methodology is cost-effective, non-toxic, generates a high yield of product, is column chromatography free and does not need the use of a specific instrument. Surprisingly, our methodology uses moderate conditions and can count the tolerance of a wide variety of electron-donating and electron-withdrawing groups. The analysis and early conclusions give more value and context for the future development of organic synthesis using photocatalysts.  The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022.</text>
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              <text>1,2,4-Triazol-3-amine; Eosin Y; Four-component synthesis; Metal-free; Multicomponent reaction; Photocatalyst; White LED</text>
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              <text>ISSN: 10225528;</text>
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              <text>English</text>
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              <text>Restricted Access; Hardcopy may be available in the library</text>
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