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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/317" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/317</id>
  <updated>2026-10-13T04:09:15Z</updated>
  <dc:date>2026-10-13T04:09:15Z</dc:date>
  <entry>
    <title>Constituents of high altitude Himalayan herbs. part XX. A C-19 diterpenoid alkaloid from Aconitum balfourii</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/701" />
    <author>
      <name>Khetwal, K S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/701</id>
    <updated>2008-04-07T04:30:27Z</updated>
    <published>2007-08-01T00:00:00Z</published>
    <summary type="text">Title: Constituents of high altitude Himalayan herbs. part XX. A C-19 diterpenoid alkaloid from Aconitum balfourii
Authors: Khetwal, K S
Abstract: A C-19 Diterpenoid alkaloid, 14-benzoylpseudaconine 1 has been isolated from the aerial parts of Aconitum balfourii and identified by MS, ¹H , ¹³C NMR (SFORD and DEPT) as well as by chemical analysis.
Page(s): 1364-1366</summary>
    <dc:date>2007-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Facile and efficient synthesis of 1,8-naphthyridinyl phthalazine-1,4-diones under microwave irradiation</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/699" />
    <author>
      <name>Mogilaiah, K</name>
    </author>
    <author>
      <name>Rani, J Uma</name>
    </author>
    <author>
      <name>Babu, H Sharath</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/699</id>
    <updated>2008-04-21T04:30:32Z</updated>
    <published>2007-08-01T00:00:00Z</published>
    <summary type="text">Title: Facile and efficient synthesis of 1,8-naphthyridinyl phthalazine-1,4-diones under microwave irradiation
Authors: Mogilaiah, K; Rani, J Uma; Babu, H Sharath
Abstract: Microwave irradiation of 3-aryl-2-hydrazino-1,8-naphthyridines 1 with phthalic anhydride 2 in the presence of a catalytic amount of DMF provides a fast, efficient and simple method for the synthesis of 2-(3-aryl-1,8-naphthyridin-2-yl)-1,2,3,4-tetrahydrophthalazine-1,4-diones 3 in excellent yields.
Page(s): 1361-1363</summary>
    <dc:date>2007-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Essential oil composition of Gliricidia sepium (Leguminosae) leaves and flowers</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/698" />
    <author>
      <name>Kaniampady, Molykutty M</name>
    </author>
    <author>
      <name>Arif, M Muhammed</name>
    </author>
    <author>
      <name>Jirovetz, L</name>
    </author>
    <author>
      <name>Shafi, P Mohamed</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/698</id>
    <updated>2008-04-07T04:30:27Z</updated>
    <published>2007-08-01T00:00:00Z</published>
    <summary type="text">Title: Essential oil composition of Gliricidia sepium (Leguminosae) leaves and flowers
Authors: Kaniampady, Molykutty M; Arif, M Muhammed; Jirovetz, L; Shafi, P Mohamed
Abstract: Forty two known compounds have been found in the leaves and flowers of Gliricidia sepium. Of these, sixteen have been identified and quantified from the leaf essential oil by GC and twenty six have been identified and quantified from the flower essential oil by GC-MS analysis. The major compounds of the leaf oil are found to be propyleneglycol (25.1%), coumarin (18.2%), (Z)-3-hexenol] (17.7%), β-farnesene (14.2%) and (E)-2-hexenol (6.5%); and coumarin (43.1%), hydroquinone (21.6%) and myrtenol (12.7%) in the flower oil. In the light of the toxicity of coumarin and hydroquinone, this finding is a warning signal against the use of the leaves as fumigant against mosquitoes and the flower as a food material.
Page(s): 1359-1360</summary>
    <dc:date>2007-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Pyrrolidine catalyzed regioselective and diastereoselective direct aldol reaction in water</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/697" />
    <author>
      <name>Mahajan, Dinesh</name>
    </author>
    <author>
      <name>Chimni, Swapandeep Singh</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/697</id>
    <updated>2008-04-09T04:30:25Z</updated>
    <published>2007-08-01T00:00:00Z</published>
    <summary type="text">Title: Pyrrolidine catalyzed regioselective and diastereoselective direct aldol reaction in water
Authors: Mahajan, Dinesh; Chimni, Swapandeep Singh
Abstract: Pyrrolidine catalyzed direct aldol reaction of methyl ketones other than acetone with 4-nitrobenzaldehyde in water affords linear aldol addition product arising from the selective attack of the unsubstituted carbon of the unsymmetrical ketone. The present methodology provides an experimentally simple and green process for regioselective synthesis of -hydroxyketones in water.
Page(s): 1355-1358</summary>
    <dc:date>2007-08-01T00:00:00Z</dc:date>
  </entry>
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