The light induced ring closure of cycloheptatrienes to bicycle-[3,2,0]-hepta-2,6-dienes is generally directionally specific in those cases where theoretically two bicyclic products may be formed (1). We have recently rationalised this fact in terms of the effect of eubstituents on the dirdction of p
A decisive electronic effect of a bridgehead methoxy substituent on the electrophilic cage opening of 1,3-bishomocubanones
✍ Scribed by A.J.H. Klunder; G.J.A. Ariaans; B. Zwanenburg
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 272 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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