Recent studies at Durham on direct fluorination

Citation
Rd. Chambers et al., Recent studies at Durham on direct fluorination, J FLUORINE, 100(1-2), 1999, pp. 63-73
Citations number
28
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF FLUORINE CHEMISTRY
ISSN journal
00221139 → ACNP
Volume
100
Issue
1-2
Year of publication
1999
Pages
63 - 73
Database
ISI
SICI code
0022-1139(199912)100:1-2<63:RSADOD>2.0.ZU;2-1
Abstract
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.