Stereoconvergent ‘one-pot’ tandem [2,3]-Wittig-anionic oxy-Cope rearrangement of acyclic bis-allylic ethers in the diastereoselective synthesis of substituted tetrahydropyrans
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940001469
Reference13 articles.
1. T.-L. Ho , Tandem Organic Reactions, Wiley, New York, 1992.
2. Acyclic Stereocontrol via [2,3]-Wittig Sigmatropic Rearrangement
3. Stereocontrolled Construction of Complex Cyclic Ketones via Oxy-Cope Rearrangement
4. Acyclic diastereocontrol and asymmetric transmission via anionic oxy-Cope rearrangement: a synthetic application of sequential [2,3]Wittig-oxy-Cope rearrangements
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1. Base-Mediated Cascade Rearrangements of Aryl-Substituted Diallyl Ethers;The Journal of Organic Chemistry;2015-01-08
2. ChemInform Abstract: Stereoconvergent ′One-Pot′ Tandem (2,3)-Wittig-Anionic Oxy-Cope Rearrangement of Acyclic Bis-Allylic Ethers in the Diastereoselective Synthesis of Substituted Tetrahydropyrans.;ChemInform;2010-08-18
3. Rearrangements of Dienes and Polyenes;PATAI'S Chemistry of Functional Groups;2009-12-15
4. Sequencing Pericyclic Reactions: The Ester Dienolate [2,3]-Wittig/Oxy-Cope Rearrangement/Carbonyl Ene Reaction, a New Access to Substituted Carbocycles;European Journal of Organic Chemistry;2001-02
5. Recent applications of anionic oxy-cope rearrangements;Tetrahedron;1997-10
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