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
โฆ LIBER โฆ
The photochemistry of cycloheptatrienes - directive effect of substituents on ring closure
โ Scribed by A.R. Brember; A.A. Gorman; R.L. Leyland; J.B. Sheridan
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 240 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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