[3,3]Claisen vs. [2,3]Wittig Shift in Thermal and Fluolide Ion-Promoted Rearrangements of theO- andC-Silylated Forms of α-Allyloxy Esters
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference11 articles.
1. The anionic oxy-claisen rearrangement of enolates of .alpha.-allyloxy ketones. A remarkable rate accelerating effect exhibited by the nature of the counterion
2. Regiospecific synthesis of .beta.,.gamma.-unsaturated ketones from allylic alcohols. Claisen rearrangement of .alpha.-allyloxy ketone enol derivatives
3. The [2,3] Sigmatropic Reaction of Acetonyl Allyl Ethers, a new method for preparing certain 2-hydroxyketones
4. The [2,3]Wittig rearrangement of 2-alkenyloxyacetic acids and its applications to the stereocontrolled synthesis of β, γ-unsaturated aldehydes and conjugated dienoic acids
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1. Development of a Phase-Transfer-Catalyzed, [2,3]-Wittig Rearrangement;The Journal of Organic Chemistry;2015-10-02
2. Palladium-Catalyzed Allylic Alkylation Reactions of Glycolates as a Tool for the Synthesis of Functionalized α-Hydroxy Esters;European Journal of Organic Chemistry;2015-08-03
3. Claisen Rearrangement through Enolization of 2-Allyloxyindolin-3-ones: Construction of Adjacent Carbon Stereocenters in 3-Hydroxyindolin-2-ones;Synthesis;2010-08-13
4. γ-Silylated α,β-unsaturated amides — Preparation by [1,5]-sigmatropic rearrangement and use as masked dienolate equivalents in carbonyl condensations;Canadian Journal of Chemistry;2009-06
5. Lewis Base-Catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Carbonyl Compounds;Bulletin of the Chemical Society of Japan;2006-08
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