<?xml version="1.0" encoding="UTF-8"?>
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  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/563" />
  <subtitle />
  <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/563</id>
  <updated>2026-05-21T02:47:37Z</updated>
  <dc:date>2026-05-21T02:47:37Z</dc:date>
  <entry>
    <title>Monofunctional primary amine: A new class of organocatalyst for asymmetric Aldol reaction</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1003" />
    <author>
      <name>Vanlaldinpuia, K</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1003</id>
    <updated>2025-10-17T04:44:30Z</updated>
    <published>2017-01-13T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2017-01-13T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Monofunctional primary amine: A new class of organocatalyst for asymmetric Aldol reaction</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/992" />
    <author>
      <name>Vanlaldinpuia, K</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/992</id>
    <updated>2025-10-16T10:26:08Z</updated>
    <published>2017-01-13T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2017-01-13T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Saccharide success: exploring the role of Dfructose-based thioureas as organocatalysts for the enantioselective Friedel–Crafts alkylation reaction†</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/990" />
    <author>
      <name>Vanlaldinpuia, K</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/990</id>
    <updated>2025-10-16T10:24:25Z</updated>
    <published>2025-03-04T00:00:00Z</published>
    <summary type="text">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).</summary>
    <dc:date>2025-03-04T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Antioxidant and cytotoxic properties of Acmella oleracea</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/989" />
    <author>
      <name>Vanlaldinpuia, K</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/989</id>
    <updated>2025-10-16T10:21:57Z</updated>
    <published>2018-10-16T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2018-10-16T00:00:00Z</dc:date>
  </entry>
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