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    <title>DSpace Collection:</title>
    <link>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/563</link>
    <description />
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        <rdf:li rdf:resource="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1003" />
        <rdf:li rdf:resource="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/992" />
        <rdf:li rdf:resource="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/990" />
        <rdf:li rdf:resource="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/989" />
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    <dc:date>2026-05-21T02:46:15Z</dc:date>
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  <item rdf:about="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1003">
    <title>Monofunctional primary amine: A new class of organocatalyst for asymmetric Aldol reaction</title>
    <link>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1003</link>
    <description>Title: Monofunctional primary amine: A new class of organocatalyst for asymmetric Aldol reaction
Authors: Vanlaldinpuia, K
Abstract: A new class of organocatalysts involving a primary amine as the only functional group is developed&#xD;
for catalytic asymmetric aldol reaction of cyclohexanone/cyclopentanone with various aryl aldehydes in the&#xD;
presence of benzoic acid as an additive at −10◦C. In an unexpected observation, the primary amine catalyzed&#xD;
reactions gave excellent yield and good to excellent stereoselectivity, while secondary amines were found to&#xD;
have little or no reactivity under similar reaction conditions.</description>
    <dc:date>2017-01-13T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/992">
    <title>Monofunctional primary amine: A new class of organocatalyst for asymmetric Aldol reaction</title>
    <link>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/992</link>
    <description>Title: Monofunctional primary amine: A new class of organocatalyst for asymmetric Aldol reaction
Authors: Vanlaldinpuia, K
Abstract: A new class of organocatalysts involving a primary amine as the only functional group is developed&#xD;
for catalytic asymmetric aldol reaction of cyclohexanone/cyclopentanone with various aryl aldehydes in the&#xD;
presence of benzoic acid as an additive at −10◦C. In an unexpected observation, the primary amine catalyzed&#xD;
reactions gave excellent yield and good to excellent stereoselectivity, while secondary amines were found to&#xD;
have little or no reactivity under similar reaction conditions.</description>
    <dc:date>2017-01-13T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/990">
    <title>Saccharide success: exploring the role of Dfructose-based thioureas as organocatalysts for the enantioselective Friedel–Crafts alkylation reaction†</title>
    <link>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/990</link>
    <description>Title: Saccharide success: exploring the role of Dfructose-based thioureas as organocatalysts for the enantioselective Friedel–Crafts alkylation reaction†
Authors: Vanlaldinpuia, K
Abstract: In this study, a series of sixteen (16) D-fructose-based bifunctional thioureas were examined as&#xD;
organocatalysts for the enantioselective Friedel–Crafts alkylation of indoles and pyrrole with bnitrostyrenes. This investigation is a part of our ongoing project, which aims to expand the scope of&#xD;
application of D-fructose-based thioureas. Under the optimized low-temperature reaction conditions,&#xD;
the corresponding adducts were obtained with good yield (up to 95%) and excellent enantioselectivity&#xD;
(&gt;99% ee).</description>
    <dc:date>2025-03-04T00:00:00Z</dc:date>
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  <item rdf:about="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/989">
    <title>Antioxidant and cytotoxic properties of Acmella oleracea</title>
    <link>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/989</link>
    <description>Title: Antioxidant and cytotoxic properties of Acmella oleracea
Authors: Vanlaldinpuia, K
Abstract: Acmella oleracea has been widely used in various traditional medicines for the treatment of different diseases ranging from&#xD;
infection, helminthiasis, peptic ulcer to dental abscess. In this experiment, we analysed the antioxidant property of the&#xD;
methanol extract of A. oleracea by hydroxyl radical-scavenging assay and hydrogen peroxide-scavenging assay. In both the&#xD;
scavenging assays, the plant extract showed free radical scavenging activities in a concentration-dependent manner. The&#xD;
cytotoxic property was also determined by MTT assay, which indicated a potential cytotoxic effect on cancer cell lines such&#xD;
as HeLa (ATCC® CCL-2TM) and V79 (ATCC® CCL-93TM) cells. Higher cytotoxicity was noticed on V79 with an IC50 of 54.341&#xD;
µg/ml. The plant extract was only moderately toxic on HeLa. The results indicated that the plant contains important bioactive&#xD;
compounds having pharmacological properties.</description>
    <dc:date>2018-10-16T00:00:00Z</dc:date>
  </item>
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