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    <name>Article</name>
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              <text>UV-Promoted Metal- and Photocatalyst-Free Direct Conversion of Aromatic Aldehydes to Nitriles</text>
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              <text>aldehydes; catalyst-free; green chemical synthesis; nitriles; UV light</text>
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              <text>Abstract: An efficient, simple, and catalyst-free UV-induced functional group transformation of aromatic aldehydes to nitriles has been reported. The developed strategy delivers various functionalized aromatic nitriles with high yields and purity. The UV irradiation activates the carbonyl group of aldehydes and leads to the formation of aldoxime intermediate, further resulting in the generation of nitriles. The striking highlights of the reported methodology are simple reaction conditions, good yields, UV-promoted transformation, and catalyst-free synthesis. Due to the above-mentioned advantages, the methodology provides a whip hand toward environmentally friendly chemical synthesis.  2022, Pleiades Publishing, Ltd.</text>
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          <name>Creator</name>
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              <text>Joy F.; Peter F.; Gokul P.C.; Nizam A.; Chinnam S.</text>
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              <text>Russian Journal of Organic Chemistry, Vol-58, No. 3, pp. 379-384.</text>
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              <text>Pleiades journals</text>
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              <text>2022-01-01</text>
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              <text>&lt;a href="https://doi.org/10.1134/S1070428022030174" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1134/S1070428022030174&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128297005&amp;amp;doi=10.1134%2FS1070428022030174&amp;amp;partnerID=40&amp;amp;md5=fd812cc39290f4d9de35010773227563" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128297005&amp;amp;doi=10.1134%2fS1070428022030174&amp;amp;partnerID=40&amp;amp;md5=fd812cc39290f4d9de35010773227563&lt;/a&gt;</text>
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          <name>Rights</name>
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              <text>Restricted Access</text>
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              <text>ISSN: 10704280; CODEN: RJOCE</text>
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              <text>Online</text>
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              <text>English</text>
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              <text>Joy F., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Peter F., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Gokul P.C., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Nizam A., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Chinnam S., Department of Chemistry, B.M.S. College of Engineering, Bengaluru, 560019, India</text>
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