| Literature DB >> 22332365 |
E V Buravlev, I Iu Chukchieva, O G Shevchenko, K Iu Suponitskiĭ, A V Kuchin.
Abstract
The resolution of the racemic ortho-isobornylphenol into enantiomers via diastereomeric camphanates was carried out. The absolute configuration ofchiral centers of synthesized compounds was established by the single crystal X-ray diffraction method. Antioxidant activity and membrane protective properties of individual enantiomers were studied on the model of H2O2-induced hemolysis of red blood cells.Entities:
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Year: 2011 PMID： 22332365 DOI： 10.1134/s1068162011050049
Source DB: PubMed Journal: Bioorg Khim ISSN： 0132-3423