714957-18-3Relevant academic research and scientific papers
The synthesis of some deoxygenated analogues of early intermediates in the biosynthesis of glycosylphosphatidylinositol (GPI) membrane anchors
Dix, Alexander P.,Borissow, Charles N.,Ferguson, Michael A. J.,Brimacombe, John S.
, p. 1263 - 1277 (2007/10/03)
Syntheses are described of 2-azido-4,6-di-O-benzyl-2,3-dideoxy-D-ribo- hexopyranosyl fluoride, 6-O-acetyl-2-azido-3-O-benzyl-2,4-dideoxy-D-xylo- hexopyranosyl fluoride and 2-azido-3,4-di-O-benzyl-2,6-dideoxy-D-glucopyranosyl fluoride. These glycosyl donor
Analogues of D-glucosaminylphosphatidylinositol: Synthesis of the glycosyl donors
Dix, Alexander P.,Borissow, Charles N.,Ferguson, Michael A.J.,Brimacombe, John S.
, p. 117 - 119 (2007/10/03)
Appropriately protected deoxy and other analogues of 2-azido-2-deoxy-D-glucopyranosyl fluoride have been synthesised preparatory to inclusion into analogues of the D-glucosaminylphosphatidylinositol 1.
