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
Acid-catalyzed rearrangements of 7-oxygenated norbornenyl derivatives
โ Scribed by Vera K. Jones; Lee B. Jones
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 152 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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