<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
  <channel>
    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.47B(02) [February 2008]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/1393</link>
    <description />
    <textInput>
      <title>The Collection's search engine</title>
      <description>Search the Channel</description>
      <name>search</name>
      <link>http://nopr.niscair.res.in/simple-search</link>
    </textInput>
    <item>
      <title>Synthesis of azo compounds containing thymol moiety</title>
      <link>http://nopr.niscair.res.in/handle/123456789/1421</link>
      <description>Title: Synthesis of azo compounds containing thymol moiety
&lt;br/&gt;
&lt;br/&gt;Authors: Koshti, S M; Sonar, J P; Sonawane, A E; Pawar, Y A; Nagle, P S; Mahulikar, P P; More, D H
&lt;br/&gt;
&lt;br/&gt;Abstract: The present work includes the synthesis of azo compounds containing thymol moiety.
&lt;br/&gt;
&lt;br/&gt;Page(s): 329-331</description>
      <pubDate>Tue, 29 Jan 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>A new scalarane sesterterpene from a marine sponge Hyatella cribrifomis Hyatt of the Indian ocean</title>
      <link>http://nopr.niscair.res.in/handle/123456789/1420</link>
      <description>Title: A new scalarane sesterterpene from a marine sponge Hyatella cribrifomis Hyatt of the Indian ocean
&lt;br/&gt;
&lt;br/&gt;Authors: Kumar, M M Krishna; Krishna, N; Muralidhar, P; Sastry, B S; Rao, D Venkata
&lt;br/&gt;
&lt;br/&gt;Abstract: A new scalarane sesterterpene, 24-β-methoxyscalarolide 4, along with known scalaranes- 12-epi-deoxoscalarin 1, 12-epi-12-deacetyl-25-deoxyscalarin 2 and scalarolide 3 has been isolated from a marine sponge, Hyatella cribriformis, of the Indian ocean. The structure of compound 4 has been determined on the basis of ¹H and ¹³C NMR, DEPT, ¹H-¹H COSY and EIMS experiments.
&lt;br/&gt;
&lt;br/&gt;Page(s): 325-328</description>
      <pubDate>Tue, 29 Jan 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>p-TsOH Catalyzed regioselective synthesis of 8,8'-methylene-bis-4- oxo-dihydrochromeno [4,3-c]pyrazoles</title>
      <link>http://nopr.niscair.res.in/handle/123456789/1419</link>
      <description>Title: p-TsOH Catalyzed regioselective synthesis of 8,8'-methylene-bis-4- oxo-dihydrochromeno [4,3-c]pyrazoles
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, Ch Sanjeeva; Nagaraj, A
&lt;br/&gt;
&lt;br/&gt;Abstract: The ethyl-5-[3-(ethoxycarbonyl)-4-hydroxybenzyl]- 2-hydroxybenzoate 3 is prepared by the usual esterification of 5-(3-carboxy-4-hydroxybenzyl)-2-hydroxy benzoic acid 2. Compound 3 on reacting with ethyl acetoacetate yields 3-acetyl-6-[(3-acetyl-4-hydroxy-2-oxo-2H-6- chromenyl)methyl]-4-hydroxy-2H-2-chromenone 4. The regioselective conversion, by cyclizing the hydrazone 5 of compound 4 to either 8,8'-methylene-bis-4-oxo-1,4-dihydrochromeno [4,3-c]pyrazoles 6 with p-toluene sulfonic acid in refluxing xylene or 8,8'-methylene-bis-4-oxo-2,4-dihydro chromeno[4,3-c]pyrazoles 7 with corresponding hydrazine hydrochloride in refluxing acetic acid is described.
&lt;br/&gt;
&lt;br/&gt;Page(s): 319-324</description>
      <pubDate>Tue, 29 Jan 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Ceric ammonium nitrate (CAN) promoted efficient solid phase synthesis of amide derivatives: A green approach</title>
      <link>http://nopr.niscair.res.in/handle/123456789/1418</link>
      <description>Title: Ceric ammonium nitrate (CAN) promoted efficient solid phase synthesis of amide derivatives: A green approach
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, Ch Sanjeeva; Raghu, M; Nagaraj, A
&lt;br/&gt;
&lt;br/&gt;Abstract: Ceric ammonium nitrate (CAN) has been found to be an efficient catalyst for the solid phase synthesis of amide derivatives of a wide range of substituted carboxylic acids and urea in excellent yields under microwave irradiation conditions. High yields are achieved even on a gram scale, while reaction times are considerably shortened. This method displays both economic and environmental advantages.
&lt;br/&gt;
&lt;br/&gt;Page(s): 315-318</description>
      <pubDate>Tue, 29 Jan 2008 22:58:59 GMT</pubDate>
    </item>
  </channel>
</rss>

