Eur. J. Chem. volume 6, issue 3, P305-313 2015 DOI: 10.5155/eurjchem.6.3.305-313.1268 View Full Text
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Huma Aslam Bhatti, Nizam Uddin, Khurshid Ayub, Bibi Saima, Maliha Uroos, Jamshed Iqbal, Shazia Anjum, Mark Edward Light, Abdul Hameed, Khalid Mohammed Khan

Abstract: We describe the oxidation of flavanones by employing phenyliodonium diacetate to form the flavone (15), isoflavone (8) and 2,3-dihydrobenzofurane (18) in this study. The oxidative method was found to be regioselective and dependent on the substitution pattern present on the two aromatic rings of the starting flavanone. The structures of products obtained were fully characterized by using IR, 1 H and 13 C NMR spectroscopy and Mass spectrometry. X-ray crystallography further confirms the structures of flavones a…

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