Reactivity and π-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 π-facial selectivity of MeOH and H 2 O addition to
Reactivity and π-facial selectivity of nucleophile addition to the radical cations of 7-benzhydrylidenenorbornene derivatives
✍ Scribed by Hideki Ishii; Satoshi Shiina; Takashi Hirano; Haruki Niwa; Mamoru Ohashi
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 258 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
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 investigated.
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