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<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0" article-type="general-sciences" lang="en"><front><journal-meta><journal-id journal-id-type="publisher">IJCRR</journal-id><journal-id journal-id-type="nlm-ta">I Journ Cur Res Re</journal-id><journal-title-group><journal-title>International Journal of Current Research and Review</journal-title><abbrev-journal-title abbrev-type="pubmed">I Journ Cur Res Re</abbrev-journal-title></journal-title-group><issn pub-type="ppub">2231-2196</issn><issn pub-type="opub">0975-5241</issn><publisher><publisher-name>Radiance Research Academy</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1314</article-id><article-id pub-id-type="doi"/><article-id pub-id-type="doi-url"/><article-categories><subj-group subj-group-type="heading"><subject>General Sciences</subject></subj-group></article-categories><title-group><article-title>BENZOPHENONE SENSITIZED ONE-POT PHOTOREDOX REACTION OF N-(__ampersandsignAlpha;-CYANO-__ampersandsignAlpha;-SUBSTITUTED PHENYL)-METHYLANILINES LEADING TO THE SYNTHESIS OF BENZOIMIDAZOLOQUINOLINES&#13;
</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Kaur</surname><given-names>Manpreet</given-names></name></contrib><contrib contrib-type="author"><name><surname>Singh</surname><given-names>Baldev</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><day>18</day><month>06</month><year>2013</year></pub-date><volume>)</volume><issue/><fpage>1</fpage><lpage>9</lpage><permissions><copyright-statement>This article is copyright of Popeye Publishing, 2009</copyright-statement><copyright-year>2009</copyright-year><license license-type="open-access" href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.</license-p></license></permissions><abstract><p>N-(__ampersandsignalpha;-cyano-__ampersandsignalpha;-substituted phenyl)-methylanilines (I) on exposure to bright sunlight using soda glass photoreactor are transformed smoothly, with insertion of one methylene group from the solvent (methanol), into substituted benzoimidazoloquinolines (II) with improved yields under benzophenone sensitized conditions employing basic aqueous alcoholic medium in the presence of iodide salt. These compounds have been characterized through their, elemental analysis, IR, 1H NMR, 13C NMR and mass spectral studies.&#13;
</p></abstract><kwd-group><kwd>Azomethines</kwd><kwd> N-(?-cyano-?-substituted phenyl)-methylanilines</kwd><kwd> benzophenone</kwd></kwd-group></article-meta></front></article>
