Oxidation of zeaxanthin: Isolation and properties of 3-hydroxyretinene |
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Authors: | R. K. Barua and A. B. Barua |
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Affiliation: | Department of Chemistry, University of Gauhati, Gauhati 14, Assam, India |
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Abstract: | 1. Anthers of Delonix regia flowers are a rich source of zeaxanthin. 2. Oxidation of zeaxanthin with hydrogen peroxide in the presence of osmium tetroxide results in the formation of 3-hydroxyretinene as one of the products. 3. 3-Hydroxyretinene gives 3-acetoxyretinene with acetic anhydride, and an oxime with hydroxylamine hydrochloride. 4. Reduction of 3-hydroxyretinene with sodium borohydride yields 3-hydroxyvitamin A. 5. Treatment of 3-hydroxyvitamin A with dry ethanolic hydrogen chloride results in the formation of 3-ethoxyanhydrovitamin A (anhydrovitamin A2) and a compound that resembles naturally occurring anhydrovitamin A2. |
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