@article { ISI:000227051000004,
	title = {The chemical synthesis of 2-deoxy-2-fluorodisaccharide probes of the hen egg white lysozyme mechanism},
	journal = {CARBOHYDRATE RESEARCH},
	volume = {340},
	number = {3},
	year = {2005},
	month = {FEB 28},
	pages = {379-388},
	abstract = {2,4-Dinitrophenyl 2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1{\textendash}>4)-2-deoxy-2-fluoro-beta- D-glucopyranoside (GN2FG-DNP) and 2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1{\textendash}>4)-2-deoxy-2-fluoro-p-D-g lucopyranosyl fluoride (GN2FG-F) were prepared using a divergent synthetic approach involving 10 steps. The key steps involved the preparation of 1-O-acetyl-3,6-di-O-benzyl-2-deoxy-2-fluoro-alpha/beta-D-glueopyranose using Selectfluor(TM) in the presence of acetic acid and the subsequent glycosylation of this acceptor to generate the core 2-fluorodisaccharide. After further elaboration, the target molecules were obtained and tested as probes of the mechanism of hen egg white lysozyme (HEWL). Compound GN2FG-DNP is not a substrate for the enzyme while compound GN2FG-F is cleaved slowly with an apparent K., greater than 5 mM and a second-order rate constant of k(cat)/ K-m = 9.6 s(-1) M-1. Comparison of this value to that estimated for the hydrolysis of beta-chitobiosyl fluoride by HEWL (1200 s(-1) M-1) {[}Ballardie, F. W.; Capon, B.; Cuthbert, M. W.; Dearie, W. M. Bioorg. Chem. 1977, 6, 483-509] revealed a 126-fold rate decrease upon substitution of a fluorine group for the 2-acetamido group of beta-chitobiosyl fluoride. This decrease resulted in the steady-state accumulation of an intermediate as visualized by mass spectrometry and the ultimate crystallographic determination of its structure {[}Vocadlo, D. J.; Davies, G. J.; Laine, R.; Withers, S. G. Nature 2001, 412, 835-838]. (C) 2005 Elsevier Ltd. All rights reserved.},
	issn = {0008-6215},
	doi = {10.1016/j.carres.2004.12.015},
	author = {Vocadlo, DJ and Withers, SG}
}
