Developments in direct fluorination are described, which changed our percep
tion of the viability of this methodology for selective introduction of car
bon-fluorine bonds. Use of acids as solvent media is a valuable technique f
or electrophilic fluorination, especially with aromatic systems. Fluorinati
ons of 1,3-dicarbonyl compounds proceed well and techniques for promoting r
eactivity in other carbonyl derivatives are described. 'In-situ' formation
of other reagents, e.g. by reaction of fluorine with other halogens and wit
h water, provides convenient methodology for halogenation and oxidation. (C
) 1999 Elsevier Science S.A. All rights reserved.