The reduction of perylene radical cation by nucleophilic addition
β Scribed by Ted R. Evans; L.F. Hurysz
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 158 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
For correlating a homoconjugation structure of a radical cation to its reactivity with a nucleophile, the reactivity and rr-facial selectivity of CH3OH and H20 addition to the radical cations of 7-benzhydrylidenenorbornene derivatives generated by photoinduced electron transfer reactions were invest
Reactivity and Ο-Facial Selectivity of Nucleophile Addition to the Radical Cations of 7-Benzhydrylidenenorbornene Derivatives. -For correlating a homoconjugation structure of a radical cation to its reactivity with a nucleophile, the reactivity and Ο-facial selectivity of MeOH and H 2 O addition to