P. K. Garg, S. Garg, M. R. Zalutsky, G. Bioconjuate-chem-vaidyanathan, and M. R. Zalutsky, Fluorine-18 labeling of monoclonal antibodies and fragments with preservation of immunoreactivity, Bioconjugate Chemistry, vol.2, issue.1, pp.44-352, 1991.
DOI : 10.1021/bc00007a008

C. Shiue, A. Wolf, and J. Hainfeld, Synthesis of 18F-labelled N-(p-[18F]fluorophenyl)maleimide and its derivatives for labelling monoclonal antibody with 18F, Journal of Labelled Compounds and Radiopharmaceuticals, vol.26, issue.1-12, pp.287-289, 1998.
DOI : 10.1002/jlcr.2580210607

E. Schirrmacher, B. Waengler, M. Cypryk, G. Bradtmoeller, M. Schaefer et al., 18F-Labeling of Peptides by means of an Organosilicon-Based Fluoride Acceptor, 38) Pacak, J.; Tocik, pp.6047-6082, 1969.
DOI : 10.1002/anie.200600795

J. Adamson, A. B. Foster, L. D. Hall, R. N. Johnson, and R. H. Heese, Fluorinated carbohydrates, Carbohydrate Research, vol.15, issue.3, p.351, 1970.
DOI : 10.1016/S0008-6215(00)80451-6

W. Korytnyk, S. Valentekovic-horvath, C. R. Petrie, and M. Adam, A convenient synthesis of 1,2-difluoro-1, 2-dideoxyhexoses using xenon fluoride, Tetrahedron, vol.38, issue.16, pp.2547-730, 1982.
DOI : 10.1016/0040-4020(82)85090-4

K. Hamacher, Phase-transfer catalysed synthesis of 4-S-??-d-glucopyranosyl-4-thio-d-glucopyranose (thiocellobiose) and 2-S-??-d-glucopyranosyl-2-thio-d-glucopyranose (thiosophorose), Carbohydrate Research, vol.128, issue.2, p.291, 1984.
DOI : 10.1016/0008-6215(84)85336-7

P. Kovac, A short synthesis of 2-deoxy-2-fluoro-d-glucose, Carbohydrate Research, vol.153, issue.1, p.168, 1986.
DOI : 10.1016/S0008-6215(00)90209-X

D. M. Mackie, A. Maradufu, A. S. Perlin, M. Dowlut, D. G. Hall et al., Rotational isomerism about the C-5???C-6 bond of 6-O-trityl derivatives of aldohexopyranoses, and of analogs of d-galactopyranose modified at C-4, Carbohydrate Research, vol.150, issue.1, pp.23-113, 1986.
DOI : 10.1016/0008-6215(86)80003-9

. Le-glycoside-128, 50 mg ; 0,12 mmoles) et l'alcyne 117 (42 mg ; 0,12 mmoles) sont mis réaction selon le protocole général et le traitement 2 est appliqué

1. and H. Gly, 01 (ddd, 1H, J 4-5 = 10,0, J 5-6 = 2,0, J 5-6' = 3,5 Hz, H-5), 1H, J 6-6' = 12,5 Hz, p.891218293655, 2005.