Abstract
1. The reaction of sterically hindered p-hydroxycarbonyl compounds with organophosphorus compounds with labile P-H bonds leads to the formation of phosphorus-containing sterically hindered phenols whose oxidation leads to the formation of relatively stable phenoxyl radicals. 2. A diastereomeric effect is seen in the ESR spectra when the radicals have two asymmetric centers.
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Schedule a callMore From: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
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