The saturation transfers which were observed during the 'H NOE difference measurements prove an orrho + ortho 2,4-cyclohexadiene-l-one rearrangement of the reaction product of 2,6-di-fert-butyl-4-chlorophenol and 2,6dichlorobenzoquinone N-chloroimine. This process is an intramolecular rearrangement.
The reactions of 2,4- and 2,5-cyclohexadiene-1-carboxylates with base. Studies related to the mechanism of the tropolone rearrangement
✍ Scribed by Ronald M. Magid; Charles R. Grayson; Donald R. Cowsar
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 190 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
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