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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/61521</link>
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    <pubDate>Sun, 11 Oct 2026 00:19:22 GMT</pubDate>
    <dc:date>2026-10-11T00:19:22Z</dc:date>
    <item>
      <title>Green synthesis of 5-methylpyridinium derivatives by C2-functionalization of pyridine-1-oxide derivatives and their antibacterial activity</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/61547</link>
      <description>Title: Green synthesis of 5-methylpyridinium derivatives by C2-functionalization of pyridine-1-oxide derivatives and their antibacterial activity
Authors: Dhadda, Surbhi; Goswami, Prakash G; Yadav, Kalpana; Guleria, Anjali; Jangid, Dinesh K; Khandelwal, Chandra L
Abstract: An innovative green economic route has been developed for one pot multicomponent synthesis of 5-methylpyridinium&#xD;
derivatives by the reaction of 3-methylpyridine-1-oxide, aromatic aldehyde and β-ketoester catalysed by different ionic&#xD;
liquids (ILs), [BMIM][OH], [BMIM][Cl], [BMIM][Ac] in good to excellent yields. A relative study reinforced that&#xD;
[BMIM][OH] is the best IL for this C2-functionsalization reaction. The main highlights of this synthetic protocol are simple&#xD;
work-up, cost effectiveness and environmentally benign processing. The synthesized derivatives have been assessed for&#xD;
possible antibacterial activity against Staphylococcus aureus and Escherichia coli by using the microdilution method. The&#xD;
results of antibacterial activity suggests that compound 4I shows best antibacterial activity and other compounds show good&#xD;
to moderate activity.
Page(s): 185-195</description>
      <pubDate>Wed, 01 Mar 2023 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/61547</guid>
      <dc:date>2023-03-01T00:00:00Z</dc:date>
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    <item>
      <title>NiWO4 catalyzed expeditious synthesis of pyranopyrazoles</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/61546</link>
      <description>Title: NiWO4 catalyzed expeditious synthesis of pyranopyrazoles
Authors: Godinho, Mesira; Salgaonkar, Lalitprabha N; Anvekar, Tushar S; Vaz, Teotone; Kadam, Hari K
Abstract: In this paper, a multicomponent green rapid method for synthesis of pyranopyrazoles is reported using NiWO4 in water&#xD;
in 15 min. Environment friendly features such as energy efficiency, aqueous medium, no hazardous solvent, no&#xD;
chromatography, in addition to the short reaction time, catalyst reusability and substrate tolerance without affecting yield&#xD;
proves the near perfectness of this method for synthesis of medicinally important pyranopyrazoles. NiWO4, ZnWO4 and&#xD;
CuWO4 have been synthesized using extract of plant Phyllantus amarus. The prepared catalysts have been characterized by&#xD;
XRD, EDX and SEM.
Page(s): 196-201</description>
      <pubDate>Wed, 01 Mar 2023 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/61546</guid>
      <dc:date>2023-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Anti-inflammatory, analgesic and antitubercular activity of 4,6-diphenyl-4,5,6, 7-tetrahydro-3-selena-1,2,5-triazo-indene derivativesS</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/61544</link>
      <description>Title: Anti-inflammatory, analgesic and antitubercular activity of 4,6-diphenyl-4,5,6, 7-tetrahydro-3-selena-1,2,5-triazo-indene derivativesS
Authors: Balasubramanian, S; Jayalakshmi, N
Abstract: Several 4,6-diphenyl-4,5,6,7-tetrahydro-3-selena-1,2,5-triazo-indene derivatives have been synthesized by the Mannich reaction (condensation) of ethyl methyl ketone, substituted aldehyde and ammonium acetate and selenium dioxide. The chemical structures have been confirmed by means of IR, 1H NMR and mass spectral data. The synthesized compounds have been evaluated for anti-inflammatory, analgesic and antitubercular activity. The compounds have emerged as the most promising active compounds to that of standards. In addition, the inhibition effect increases with the increase in concentration of these compounds.
Page(s): 202-206</description>
      <pubDate>Wed, 01 Mar 2023 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/61544</guid>
      <dc:date>2023-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>A novel approach to determine anti-proliferative, anti-migratory and anti-microbial properties of 2-phenylethylammonium carboxylate molecular salts</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/61543</link>
      <description>Title: A novel approach to determine anti-proliferative, anti-migratory and anti-microbial properties of 2-phenylethylammonium carboxylate molecular salts
Authors: Akbaş, Hüseyin; Tayhan, Seçil Erden; Bilgin, Sema
Abstract: 2-Phenylethylammonium (PEA) salt derivatives have been prepared between 2-phenylethylamine with various&#xD;
aromatic carboxylic acids (nicotinic, benzoic, salicylic, and γ-resorcylic) and confirmed by spectroscopic analyses.&#xD;
Additionally, the possible biological activities of these salts have been examined and the antiproliferative and antimigrative&#xD;
effects of salts on breast and colon cancer cell lines have been determined. Furthermore, to obtain preliminary data for the&#xD;
effects of the indicated compounds on cancer angiogenesis, in vitro migration analysis has been performed by human&#xD;
vascular endothelial cells. The antibacterial effects of the compounds have also been investigated. Therefore, an important&#xD;
contribution has been made to studies conducted to better recognize the pharmacological effects of salts.
Page(s): 207-216</description>
      <pubDate>Wed, 01 Mar 2023 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/61543</guid>
      <dc:date>2023-03-01T00:00:00Z</dc:date>
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