An unexpected aromatization reaction during the preparation of 1,2-cyclohexanedione ethers
Abstract
Abstract
In a heretofore-unreported reaction, 1,2-cyclohexandione reacts with a variety of alcohols under mild acid-catalyzed dehydration conditions to afford not only ethers of 1,2- cyclohexanedione but the corresponding aryl ethers as well in moderate to good yield.
Citation:
Deangelis, R., & Solinski, A. (n.d.). An unexpected aromatization reaction during the preparation of 1,2-cyclohexanedione ethers. Organic Communications, 10(1), 1–5.
Description
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