Recent highlights in electrophilic fluorination with 1-chloromethyl-4-fluoro- 1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate).
Rajendra P Singh, Jean'ne M Shreeve
文献索引:Acc. Chem. Res. 37 , 31-44, (2004)
全文:HTML全文
摘要
Synthetic and structural aspects of organofluorine compounds continue to be the focal points of vigorous research activities, as evidenced by the appearance of a large number of publications. Among the various useful methodologies for the introduction of fluorine into organic molecules, electrophilic fluorination is a promising and exciting area of research. While a variety of electrophilic fluorinating reagents are available, currently 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor) provides a remarkably straightforward and effective route. The breadth of applications realizable from this reagent in its role as a key electrophilic fluorinating reagent is highlighted here. This Account covers the literature for electrophilic fluorination reactions that employ Selectfluor during the period January 1999-January 2003.
相关化合物
相关文献:
2002-01-01
[Chem. Rev. 96 , 1737, (1996)]
2004-12-27
[Angew. Chem. Int. Ed. Engl. 44 , 192, (2004)]
L.G. Sankar
[J. Org. Chem. 58 , 2791, (1993)]
D.P. Matthews et al.
[Tetrahedron Lett. 34 , 3057, (1993)]
R.E. Banks et al.
[J. Chem. Soc. Chem. Commun. , 343, (1994)]