@article { ISI:A1994PU99900002,
	title = {A SHORT SYNTHESIS OF BETA-XYLOBIOSIDES},
	journal = {CARBOHYDRATE RESEARCH},
	volume = {265},
	number = {1},
	year = {1994},
	month = {DEC 2},
	pages = {9-17},
	abstract = {Benzyl 2,3,2{\textquoteright},3{\textquoteright},4{\textquoteright}-penta-O-acetyl-beta-xylobioside, 2-nitrophenyl beta-xylobioside, 4-nitrophenyl beta-xylobioside, and 2-iodobenzyl 1-thio-beta-xylobioside were synthesized via a short and highly selective route. beta-D-Xylopyranosides were selectively 4-O-triethylsilylated using dibutyltin oxide and triethyhilyl chloride and subsequently 2,3-di-O-acetylated. Desilylation under acidic conditions gave the 4-unprotected xylosides which then were beta-D-xylosylated using 2,3,4-tri-O-acetyl-alpha-D-xylopyranosyl trichloroacetimidate.},
	issn = {0008-6215},
	doi = {10.1016/0008-6215(94)00214-2},
	author = {ZISER, L and Withers, SG}
}
