Selective, electrophilic fluorinations using N-fluoro-o-benzenedisulfonimide
FA Davis, W Han, CK Murphy
Index: Davis, Franklin A.; Han, Wei; Murphy, Christopher K. Journal of Organic Chemistry, 1995 , vol. 60, # 15 p. 4730 - 4737
Full Text: HTML
Citation Number: 146
Abstract
The synthesis of N-fluoro-o-benzenedisulfonimide (NFOBS, 2) and its use as an “electrophilic” fluorinating reagent with nucleophilic substrates is described and compared with that of N-fluorobenzenesulfonimide (NFSi, 3). NFOBS (2) is prepared in three steps in 81% overall yield from commercially available o-benzenedisulfonic acid (4) and involves treatment of o-benzenedisulfonimide (6) with dilute fluorine (10% Fflz). Reaction of 2 with ...
Related Articles:
[Kiddle, James J.; Gurley, Alison F. Phosphorus, Sulfur and Silicon and Related Elements, 2000 , vol. 160, p. 195 - 205]
[Journal of Fluorine Chemistry, , vol. 92, # 1 p. 45 - 52]
[Kvicala, Jaroslav; Vlasakova, Ruzena; Plocar, Jakub; Paleta, Oldrich; Pelter, Andrew Collection of Czechoslovak Chemical Communications, 2000 , vol. 65, # 5 p. 772 - 788]
[Synthetic Communications, , vol. 24, # 9 p. 1317 - 1322]
[Justus Liebigs Annalen der Chemie, , vol. 693, p. 134 - 157]