Binkley, Roger W.; Hehemann, David G. published an article in 1978, the title of the article was New synthesis of deoxyiodo sugars.Recommanded Product: 38838-06-1 And the article contains the following content:
Five deoxyiodo sugars were synthesized by reaction of partially protected monosaccharides with (CF3SO2)2O to produce the corresponding triflate derivatives, which are converted to the deoxyiodo compounds by reaction with Bu4N+ I-. These reactions are convenient, with no competing elimination or rearrangement processes, and the product yields are 65-99%. This reaction sequence provides the first synthesis of 3-deoxy-3-iodo-1,2:5,6-di-O-isopropylidene-α-D-allofuranose (I). Previous attempts to synthesize I have resulted in rearrangement reactions. The experimental process involved the reaction of (3aS,4S,6R,6aR)-4-(Iodomethyl)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole(cas: 38838-06-1).Recommanded Product: 38838-06-1
The Article related to sugar deoxyiodo, iododeoxypentose, pentose iododeoxy, hexose iododeoxy, Carbohydrates: Monosaccharides, Glycals and other aspects.Recommanded Product: 38838-06-1
Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem