Solvent Effect on the Rearrangement of Cyclohexanoneoxime-p-toluenesulfonate. The Ionizing Power of Liquid Sulfur Dioxide
- 1 February 1964
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 37 (2) , 138-144
- https://doi.org/10.1246/bcsj.37.138
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- The Acid-Catalyzed Isomerization of Cyclohexyl Phenyl Ketoxime in Liquid Sulfur DioxideBulletin of the Chemical Society of Japan, 1962
- Isomerization of Cyclohexyl Phenyl Ketoxirne in Liquid Sulfur DioxideBulletin of the Chemical Society of Japan, 1962
- Beckmann Rearrangement. III. Rearrangement of Oxime p-Toluenesulfonates in Chloroform, Acetic Acid, and MethanolThe Journal of Organic Chemistry, 1961
- The Beckmann Rearrangement of the Geometrical Isomers of Cyclohexyl Phenyl Ketoxime in Liquid Sulfur DioxideBulletin of the Chemical Society of Japan, 1961
- The Beckman Rearrangement. VIII. The Influence of Alkyl Groups on the Rates of Rearrangement of Acetophenone Oximes1Journal of the American Chemical Society, 1959
- Zum Chemismus der Arylwanderung bei der Beckmann‐Umlagerung, IIEuropean Journal of Inorganic Chemistry, 1957
- THE BECKMANN REARRANGEMENT. V. THE REARRANGEMENT RATES OF SOME ortho-SUBSTITUTED ACETOPHENONE OXIMES (1)The Journal of Organic Chemistry, 1955
- THE QUESTION OF HYPERCONJUGATION OR OF BULK EFFECT IN THE BECKMANN REARRANGEMENTThe Journal of Organic Chemistry, 1954
- Hammett's Sigma Constants in Certain Electrophilic ReactionsThe Journal of Organic Chemistry, 1952
- THE BECKMANN REARRANGEMENT. THE REARRANGEMENT OF SOME SUBSTITUTED ACETOPHENONE OXIMES IN SULFURIC ACIDThe Journal of Organic Chemistry, 1949