Four glycolipids carrying different glycans and a nitroxide free radical spin at the
glycan non-reducing end were designed and synthesized from free glucose and maltooligosaccharides
by an efficient and streamlined synthetic strategy. The main features of this synthetic
strategy include regioselective functionalization of the free carbohydrates and coupling
of the radical spin label with functionalized free glycans as the last synthetic step.
These glycolipids are useful probes for the study of cell surface glycans by electron
paramagnetic resonance spectroscopy. Moreover, the key synthetic intermediates, free
glycolipids carrying a flexible azido group at the glycan non-reducing end, are widely
useful platforms for accessing glycolipids with other molecular labels.
Key words
glycolipids - carbohydrates - glycans - nitroxides - radical spin label - electron
paramagnetic resonance spectroscopy