[2,3]Wittig Rearrangements of “Lithium Enolates” Generated from α-Allyloxy Esters, Ketones, and Oximes. Some Implications of the Enolate Structures
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference9 articles.
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3. The anionic oxy-claisen rearrangement of enolates of .alpha.-allyloxy ketones. A remarkable rate accelerating effect exhibited by the nature of the counterion
4. The [2,3] Sigmatropic Reaction of Acetonyl Allyl Ethers, a new method for preparing certain 2-hydroxyketones
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