@article {805,
	title = {Carbohydrate conjugates for molecular imaging and radiotherapy: Tc-99m(I) and Re-186(I) tricarbonyl complexes of N-(2 {\textquoteright}-hydroxybenzyl)-2-amino-2-deoxy-D-glucose},
	journal = {Bioconjugate Chemistry},
	volume = {15},
	number = {4},
	year = {2004},
	note = {ISI Document Delivery No.: 840SWTimes Cited: 39Cited Reference Count: 17},
	month = {Jul-Aug},
	pages = {923-926},
	type = {Article},
	abstract = {An approach to a new class of potential radiopharmaceuticals is demonstrated by the labeling of a glucosamine derivative with the tricarbonyls of Tc-99m and Re-186. The proligand HL2 (N-(2{\textquoteright}-hydroxybenzyl)-2-amino-2-deoxy-d-glucose) was produced by hydrogenation of the corresponding Schiff base and reacted with [NEt4](2)[Re(CO)(3)Br-3] to form the neutral complex [(L-2)Re(CO)(3)] in 40\% yield. H-1 and C-13 NMR spectra indicate that the {Re(CO)(3)} core is bound in a tridentate fashion via the amino N, phenolato O, and C-3 hydroxyl O atoms of the ligand. At the tracer-level, labeling of HL2 with [Tc-99m(CO)(3)(H2O)(3)](+) and [Re-186(CO)(3)(H2O)(3)](+) was achieved in aqueous conditions in 95 +/- 2\% and 94 +/- 3\% average radiochemical yields, respectively.},
	keywords = {BIOMOLECULES, GLUCOSE, LIGAND SYSTEMS, RADIOPHARMACEUTICALS, SUGARS},
	isbn = {1043-1802},
	url = {<Go to ISI>://000222880900032},
	author = {Bayly, S. R. and Fisher, C. L. and Storr, T. and Adam,Michael J. and Orvig, Chris}
}
@article {805,
	title = {Carbohydrate conjugates for molecular imaging and radiotherapy: Tc-99m(I) and Re-186(I) tricarbonyl complexes of N-(2 {\textquoteright}-hydroxybenzyl)-2-amino-2-deoxy-D-glucose},
	journal = {Bioconjugate Chemistry},
	volume = {15},
	number = {4},
	year = {2004},
	note = {ISI Document Delivery No.: 840SWTimes Cited: 39Cited Reference Count: 17},
	month = {Jul-Aug},
	pages = {923-926},
	type = {Article},
	abstract = {An approach to a new class of potential radiopharmaceuticals is demonstrated by the labeling of a glucosamine derivative with the tricarbonyls of Tc-99m and Re-186. The proligand HL2 (N-(2{\textquoteright}-hydroxybenzyl)-2-amino-2-deoxy-d-glucose) was produced by hydrogenation of the corresponding Schiff base and reacted with [NEt4](2)[Re(CO)(3)Br-3] to form the neutral complex [(L-2)Re(CO)(3)] in 40\% yield. H-1 and C-13 NMR spectra indicate that the {Re(CO)(3)} core is bound in a tridentate fashion via the amino N, phenolato O, and C-3 hydroxyl O atoms of the ligand. At the tracer-level, labeling of HL2 with [Tc-99m(CO)(3)(H2O)(3)](+) and [Re-186(CO)(3)(H2O)(3)](+) was achieved in aqueous conditions in 95 +/- 2\% and 94 +/- 3\% average radiochemical yields, respectively.},
	keywords = {BIOMOLECULES, GLUCOSE, LIGAND SYSTEMS, RADIOPHARMACEUTICALS, SUGARS},
	isbn = {1043-1802},
	url = {<Go to ISI>://000222880900032},
	author = {Bayly, S. R. and Fisher, C. L. and Storr, T. and Adam,Michael J. and Orvig, Chris}
}
@article {7083,
	title = {TRITERPENOID GLYCOSIDES FROM THE NORTHEASTERN PACIFIC MARINE SPONGE XESTOSPONGIA-VANILLA},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {9},
	year = {1991},
	note = {ISI Document Delivery No.: GH861Times Cited: 7Cited Reference Count: 13},
	month = {Sep},
	pages = {1352-1364},
	type = {Article},
	abstract = {Isoxestovanin A (6), xestovanin B (7), xestovanin C (8), dehydroxestovanin A (9), epidehydroxestovanin A (10), dehydroxestovanin C (11), and secodehydroxestovanin A (12), seven new triterpenoid glycosides, have been isolated from the Northeastern Pacific sponge Xestospongia vanilla. The structures of the metabolites were determined by a combination of spectroscopic analysis and chemical degradation. The aglycone of 6 has the new isoxestovanane triterpenoid carbon skeleton. Compounds 7, 8, and 11 are the first X. vanilla triterpenoid glycosides known to contain three monosaccharide subunits.},
	keywords = {C-13 ASSIGNMENTS, GLYCOSIDE, H-1, NMR, SPONGE, SUGARS, TRITERPENOID, XESTOSPONGIA},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991GH86100003},
	author = {Morris, S. A. and Northcote, P. T. and Andersen, R. J.}
}
