Abstract
Solid-phase synthesis of oligosaccharides requires the use of a saccharide derivative with a reactive leaving group at C-1, one hydroxyl protected by a readily removable blocking group, the remaining hydroxyls protected by a stable blocking group, and a resin which can be separated from the formed oligosaccharide derivative without removing the alcoholic substituents. A polystyrene resin with allyl alcohol functional groups has been prepared and a procedure for the solid-phase synthesis of oligosaccharides has been tested with an appropriately substituted glycosyl halide.
Original language | English (US) |
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Pages (from-to) | 492-496 |
Number of pages | 5 |
Journal | Journal of the American Chemical Society |
Volume | 93 |
Issue number | 2 |
DOIs | |
State | Published - Jan 1 1971 |
Externally published | Yes |
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry