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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/66985" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/66985</id>
  <updated>2026-10-10T22:20:36Z</updated>
  <dc:date>2026-10-10T22:20:36Z</dc:date>
  <entry>
    <title>Synthesis of α-hydroxy, β-bromo-exo-dicyclopentadiene-1-one: A new building block for cyclopentanoids</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/66992" />
    <author>
      <name>Kotha, Sambasivarao</name>
    </author>
    <author>
      <name>Reddy Keesari, Ramakrishna</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/66992</id>
    <updated>2025-12-24T05:41:29Z</updated>
    <published>2025-12-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis of α-hydroxy, β-bromo-exo-dicyclopentadiene-1-one: A new building block for cyclopentanoids
Authors: Kotha, Sambasivarao; Reddy Keesari, Ramakrishna
Abstract: Herein, we described a simple synthetic strategy for the preparation of α-hydroxy, β-bromo-exo-dicyclopentadiene-1-one&#xD;
by following a three-step sequence. The synthetic strategy relies on operationally simple reactions and high yielding steps.&#xD;
The newly synthesized compounds have been characterized by NMR. As the disclosed compound α-hydroxy, β-bromo-exodicyclopentadiene-&#xD;
1-one is highly functionalized but structurally similar to exo-dicyclopentadiene-1-one and it can be used a&#xD;
key building block for expanding the chemical space of cyclopentanoid derivatives.
Page(s): 1127-1132</summary>
    <dc:date>2025-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Lewis acid-promoted synthesis of 3-tosylisoindolinone from 3-hydroxyisoindolinone: Access to complex furopyrroloisoindoledione</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/66991" />
    <author>
      <name>Das, Malay</name>
    </author>
    <author>
      <name>Kumar, Virendra</name>
    </author>
    <author>
      <name>Jyoti Arandhara, Pallav</name>
    </author>
    <author>
      <name>Biswas, Subhamoy</name>
    </author>
    <author>
      <name>K Saikia, Anil</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/66991</id>
    <updated>2025-12-24T05:38:52Z</updated>
    <published>2025-12-01T00:00:00Z</published>
    <summary type="text">Title: Lewis acid-promoted synthesis of 3-tosylisoindolinone from 3-hydroxyisoindolinone: Access to complex furopyrroloisoindoledione
Authors: Das, Malay; Kumar, Virendra; Jyoti Arandhara, Pallav; Biswas, Subhamoy; K Saikia, Anil
Abstract: An efficient methodology has been developed for the synthesis of sulfur-functionalized isoindolone scaffold from&#xD;
hydroxyisoindolinone via N-acyliminium ion intermediate using TosMIC and Lewis acid in good to excellent yields. The&#xD;
strategy features mild reaction conditions, broad substrate scope and metal-free reaction method. The protocol has been&#xD;
extended for the synthesis of complex furopyrroloisoindoledione derivatives.
Page(s): 1133-1143</summary>
    <dc:date>2025-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Antituberculosis activity of α-aminoacyl amide derivatives</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/66990" />
    <author>
      <name>B Makane, Vitthal</name>
    </author>
    <author>
      <name>U Sinde, Akash</name>
    </author>
    <author>
      <name>Angayarkanni, B</name>
    </author>
    <author>
      <name>Malik, Pradip</name>
    </author>
    <author>
      <name>Chopra, Sidharth</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/66990</id>
    <updated>2025-12-24T05:35:42Z</updated>
    <published>2025-01-01T00:00:00Z</published>
    <summary type="text">Title: Antituberculosis activity of α-aminoacyl amide derivatives
Authors: B Makane, Vitthal; U Sinde, Akash; Angayarkanni, B; Malik, Pradip; Chopra, Sidharth
Abstract: The preparation and evaluation of α-aminoacyl amide derivatives against M. tuberculosis H37Rv is reported. The&#xD;
systematic modifications of hit compounds have been carried out. Compounds 19b and 19c are identified as potent and&#xD;
selective inhibitors of M. tuberculosis H37Rv with MIC 2.5 μM and 2.6 μM, respectively. Compounds 19b and 19c hold a&#xD;
promise for further development to discover new potent antituberculosis leads.
Page(s): 1144-1155</summary>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Esterification of levulinic acid with alcohol catalyzed by hierarchically porous ZSM-5 zeolites: A study on catalyst efficiency and product selectivity</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/66989" />
    <author>
      <name>Manikandan, K</name>
    </author>
    <author>
      <name>Shalini, A</name>
    </author>
    <author>
      <name>Deepa, K</name>
    </author>
    <author>
      <name>Kaladevi, G</name>
    </author>
    <author>
      <name>Valarmathi, N</name>
    </author>
    <author>
      <name>Muthuvel, I</name>
    </author>
    <author>
      <name>Thirunarayanan, G</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/66989</id>
    <updated>2025-12-24T05:31:53Z</updated>
    <published>2025-01-01T00:00:00Z</published>
    <summary type="text">Title: Esterification of levulinic acid with alcohol catalyzed by hierarchically porous ZSM-5 zeolites: A study on catalyst efficiency and product selectivity
Authors: Manikandan, K; Shalini, A; Deepa, K; Kaladevi, G; Valarmathi, N; Muthuvel, I; Thirunarayanan, G
Abstract: This study evaluates the catalytic performance of ZSM-5 zeolites synthesized using corn stem pith powder as a hard&#xD;
template in the esterification of levulinic acid with 1-proponal and heptanol. The structural and textural properties of the&#xD;
zeolites have been characterized, revealing a hierarchical porous nature. The catalytic activity of the ZSM-5 is assessed in&#xD;
the esterification of levulinic acid with 1-propanol and heptanol, yielding corresponding esters with high selectivity. The&#xD;
effects of reaction parameters, including temperature, molar ratio, catalyst loading, and reaction time, are systematically&#xD;
studied to optimize reaction conditions. The reusability and stability of the catalyst are evaluated through multiple reaction&#xD;
cycles. The results are compared with those obtained using conventional ZSM-5, highlighting the advantages of the meso&#xD;
porous structure. This study provides valuable insights into the design of hierarchical zeolite catalysts for green and&#xD;
sustainable chemistry applications. The use of corn stem pith powder as a hard template enhances the textural properties of&#xD;
the zeolite while promoting sustainability and resource efficiency.
Page(s): 1156-1163</summary>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </entry>
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