Predominant formation of 1,2-adducts during reaction of cyclooctene-S-methylepisulfonium salts with nucleophiles
β Scribed by A. S. Gybin; V. A. Smit; M. Z. Krimer
- Book ID
- 112438506
- Publisher
- Springer
- Year
- 1979
- Tongue
- English
- Weight
- 77 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1573-9171
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π SIMILAR VOLUMES
The reaction of tri-and tetrasubstituted pyrylium salts with hydroxylamine affords acyclic keto-ketoximes (to be described in a separate paper) which cyclize yielding pyridine-l-oxides and/or 2-isoxazolines. Both these classes of compounds, with many possible applications, can thus be obtained simpl
Reaction of Pyrylium Salts with Nucleophiles. Part 25. Formation of Pyridine-1-oxides, 2-Isoxazolines and 1-Pyrazoline-1-oxides. -The competitive formation of pyridine-1-oxides and 2-isoxazolines from reaction of pyrylium salts with hydroxylamine is investigated. The synthetic value of pyrylium sal
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