Author:
Gogek C. J.,Moir R. Y.,McRae J. A.,Purves C. B.
Abstract
Cyclohexene-3-ol acetate was readily made from cyclohexene and when oxidized, preferably with performic acid, gave 20 to 25% yields of partly acylated cis-cis-trans-cyclohexane-1,2,3-triol, but only 1 to 2% of the cis-trans-cis isomer. The structures of the three cyclohexane-1,2,3-triols were deduced from the theory of the Walden Inversion.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
15 articles.
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