@article { ISI:000180748300001,
	title = {Synthesis with glycosynthases: Cello-oligomers of isofagomine and a tetrahydrooxazine as cellulase inhibitors},
	journal = {AUSTRALIAN JOURNAL OF CHEMISTRY},
	volume = {55},
	number = {12},
	year = {2002},
	pages = {747-752},
	abstract = {Isofagomine and a carbohydrate-like tetrahydrooxazine, as their N-benzyloxycarbonyl derivatives, have been subjected to a glycosynthase in the presence of alpha-D-glucopyranosyl fluoride as a glucosyl donor. In each case, after protecting group removal, a mixture of 1, 4-beta-linked di-, tri-, and tetra-{\textquoteright}saccharides{\textquoteright} was obtained. These novel oligosaccharide derivatives were tested as inhibitors of the endo-glycanase Cex from Cellulomonas fimi. Affinities increased progressively as additional D-glucosyl residues were incorporated, which is consistent with the known substrate specificity of this enzyme.},
	issn = {0004-9425},
	doi = {10.1071/CH02165},
	author = {Macdonald, JM and Stick, RV and Tilbrook, DMG and Withers, SG}
}
