Abstract
Diaryl nitrones reacted with 1-hexadecene, 10-undecenoate, oleate and linoleate to yield isoxazolidines. These were reduced to amino alcohols and alcohols. Chemical degradation of some of the alcohols showed that they have straight aliphatic chains. Accordingly, the addition of diphenyl nitrone to 1-hexadecene and to 10-undecenoate led to 5-alkyl isoxazolidines. Alkyl phenols similar to cardanols were obtained from isoxazolidines that had been prepared from C-hydroxyphenyl nitrones and 1-hexadecene.
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