N-Fluoropyridinium triflate and its analogs, the first stable 1:1 salts of pyridine nucleus and halogen atom
✍ Scribed by Teruo Umemoto; Kyoichi Tomita
- Book ID
- 104218853
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 254 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
N-Fluoropyridinium salts having non-nucleophilic counter-anions and their derivatives were synthesized by treating pyridine-F 2 adducts with strong Brflnsted acids, their salts or trimethylsilyl esters, or Lewis acids, or by allowing F2 to react with N-trimethylsilylpyridinium salts.
📜 SIMILAR VOLUMES
## Abstract The complete ^1^H NMR chemical shift assignments of 1,2,3,4,5,6,7,8‐octahydroacridine (**1**), 1,2,3,4,5,6,7,8‐octahydro‐9‐(3‐pyridyl)acridine (**2**), 1,2,3,4,5,6,7,8‐octahydro‐9‐(4‐pyridyl)acridine (**3**) and the corresponding __N__(10)‐oxides **1a**, **2a** and **3a**, respectively,