[2,3] [3,3]: the novel [2,3] sigmatropic rearrangement of oxime-o-allyl ethers
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. The Wittig rearrangement of some allyl ethers
2. Molecular rearrangements related to the Claisen rearrangement
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1. Efficient synthesis of multisubstituted 2-alkenylpyridines via 2,3-rearrangement of O-homoallenylic oximes;Organic Chemistry Frontiers;2017
2. Copper-Catalyzed Skeletal Rearrangements ofO-Propargylic Oximes via Cleavage of a Carbon-Oxygen Bond;The Chemical Record;2015-02-24
3. Selective Synthesis of Allylated Oxime Ethers and Nitrones Based on Palladium-Catalyzed Allylic Substitution of Oximes;The Journal of Organic Chemistry;2005-06-09
4. Palladium (II) catalysed tandem [2,3]-sigmatropic shift-1,3-dipolar cycloaddition processes in oxime O-allyl ethers;Tetrahedron Letters;1991-01
5. A CHEMICAL AND THERMOCHEMICAL STUDY OF NON-OBSERVED SYMMETRY ALLOWED REACTIONS;R.B. Woodward Remembered;1982
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