<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>715</id><JournalTitle>SYNTHESIS OF AZOMETHINE DISELENIDES: A NEW CLASS OF  POTENT ANTIOXIDANTS</JournalTitle><Abstract>Azomethine  diselenides were prepared by a simple and convenient method employing non-cryogenic condition. The 
diselenide anion, Se
2
2-formed by reducing elemental  selenium  with 100% hydrazine hydrate in sodium hydroxide as a base 
reacts  insitu  with  2-bromobenzaldehyde  followed  by  the  condensation  with  arylamines  to  affords  the  title  compounds  in 
moderate to good yields. The newly synthesized compounds were characterized by spectral and elemental analysis and further 
screened  for  their  abilities  towards  antioxidant  activity  using  well  documented  in  vitro  assays.  Among  the  synthesized 
compounds, 3i bearing di-hydroxy group on the phenyl ring and 3j bearing methoxy group addition to phenolic moiety showed 
dominant antioxidant activity compare to standard BHA</Abstract><Email>drnaik_chem@yahoo.co.in</Email><articletype>Research</articletype><volume>7</volume><issue>1</issue><year>2016</year><keyword>Azomethine diselenides,Arylamines,Organoselenium compounds,Antioxidant activity</keyword><AUTHORS>Ashok B,Kumar Naik K.H,Nagaraja Naik</AUTHORS><afflication>Department of Chemistry, University of Mysore, Mysuru, Karnataka, India,Department of Chemistry, K.R.C.E. Societyâ€™s, G.G.D. Arts, B.M.P. Commerce and S.V.S. Science Degree College, Bailhongal, Belagavi, Karnataka, India.,Department of Chemistry, University of Mysore, Mysuru, Karnataka, India</afflication></Article></Articles>