Due to high demand to access biologically important oligosaccharide structu
res, efficient and stereoselective synthetic methods are required. This art
icle addresses these two issues from our recent studies. The first part dea
ls with P-mannosylation and cr-sialylation known as the two most difficult
glycosylation reactions which were now made possible by means of an "intram
olecular aglycon delivery" system and control by "auxiliary", respectively.
In the second part, the remarkably efficient "orthogonal glycosylation str
ategy" which was developed based on tactical analysis of oligosaccharide sy
nthesis is described.