P. Wei, R. Kerns
Oct 3, 2005
Citations
0
Influential Citations
27
Citations
Journal
Tetrahedron Letters
Abstract
Abstract These studies describe the chemoselective deprotection of trans -fused 2 N ,3 O -oxazolidinone derivatives of N -acetyl-β- d -glucosamine. Selective opening of the oxazolidinone ring or N -deacetylation without ring opening is demonstrated. Certain amines are shown to efficiently afford C-2 ureido sugars under mild conditions. This work demonstrates the high degree of chemoselective manipulation possible with ring-fused 2 N ,3 O -oxazolidinone derivatives of N -acetyl- d -glucosamine.