Abstract
A four step sequence was found to convert 2,2,6-trimethylcyclohexanone, 1, to 1-(2-hydroxyethyl)-2,6,6-trimethyl-1,3-cyclohexadiene, 2a (overall yield 76%). An efficient route to homosafranic acid 3 is also described (overall yield 80% from ketone 1).
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
9 articles.
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