Nucleophilic Perfluoroalkylation of Aldehydes, Ketones, Imines, Disulfides, and Diselenides
2006; American Chemical Society; Volume: 71; Issue: 9 Linguagem: Inglês
10.1021/jo060250j
ISSN1520-6904
AutoresChaya Pooput, William R. Dolbier, Maurice Médebielle,
Tópico(s)Inorganic Fluorides and Related Compounds
ResumoUsing a procedure analogous to that developed for nucleophilic trifluoromethylation, the perfluoroalkyl anion reagents created by mixing C2F5I and n-C4F9I with tetrakis(dimethylamino)ethylene (TDAE) were effective in their nucleophilic reactions with aldehydes, ketones, imines, disulfides, and diselenides. Irradiation proved beneficial in the aldehyde and ketone reactions.
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