The acid-catalyzed rearrangements of three model tricyclo[4.3.2] propellane derivatives have been explored. In each case the observed products are proposed to arise via a concerted 1,2-shift of the cyclobutane bond having an antiperiplanar alignment with the leaving group (i.e., stereoelectronic con
โฆ LIBER โฆ
Acid-catalyzed rearrangement of camphor to 3,4-dimethylacetophenone
โ Scribed by Rodig, Oscar R.; Sysko, Robert J.
- Book ID
- 126047360
- Publisher
- American Chemical Society
- Year
- 1972
- Tongue
- English
- Weight
- 583 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0002-7863
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