Formation and Reaction of Cyclohexanone Oxime Hydrogen Sulfate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/46/10/46_10_3168/_pdf
Reference12 articles.
1. THE BECKMANN REARRANGEMENT. THE REARRANGEMENT OF SOME SUBSTITUTED ACETOPHENONE OXIMES IN SULFURIC ACID
2. Kinetics of the Beckmann Rearrangement of Cyclohexanone Oxime
3. A Low Temperature Beckmann Rearrangement With SO3 Including Separation of Caprimidyl Sulfate as a New Composition
4. Use of Lewis base-sulfur trioxide complexes as reagents for the Beckmann rearrangement of ketoximes
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1. A General Method to Access Underexplored Ylideneamino Sulfates as Interrupted Beckmann-Type Rearrangement Intermediates;Molecules;2024-04-08
2. Sulfur Trioxide-1,4-Dioxane;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
3. The Beckmann Reactions: Rearrangements, Elimination-Additions, Fragmentations, and Rearrangement-Cyclizations;Organic Reactions;1988-05-09
4. ChemInform Abstract: FORMATION AND REACTION OF CYCLOHEXANONE OXIME SULFATE;Chemischer Informationsdienst;1973-12-25
5. Reaction of 3,4,5,6,-Tetrahydro-2H-azepin-7-ol Hydrogen Sulfate with Cyclohexanone Oxime–Tin Tetrachloride Complex;Bulletin of the Chemical Society of Japan;1973-10
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