Nucleophilic addition of azoles to triphenyl-(phenylethynyl)phosphonium bromide and base hydrolysis of the addition products
โ Scribed by G. B. Bagdasaryan; P. S. Pogosyan; G. A. Panosyan; G. V. Asratyan; M. G. Indzhikyan
- Book ID
- 111458989
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 41 KB
- Volume
- 76
- Category
- Article
- ISSN
- 1070-3632
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๐ SIMILAR VOLUMES
The chemiluminescent reaction of an acridinium ester (AE) requires addition of peroxide to the 9 position of the acridinium ring. The addition of a hydroxide ion t o the 9 position of an acridinium ester t o form the carbinol adduct has also been well documented. We have observed a similar addition
## 4, ' ) ' ) For solvent isotope effects in acid/base equilibria, see [lo]. For structural reasons, through-space interactions are negligible in such compounds. A steric effect was not detected by X-ray analysis. The interaction diagram was constructed according to the usual theoretical consider