A straightforward α-selective aromatic glycosylation and its application for stereospecific synthesis of 4-methylumbelliferyl α-T-antigen
-
Add time:07/28/2019 Source:sciencedirect.com
A practical and efficient α-selective aromatic glycosylation with simple per-O-acetyl glycopyranosyl trichloroacetimidates is reported. The method is particularly effective for L-fucosyl and 2-azido-2-deoxy-d-galatosaminyl imidates, with which exclusive α-selectivity was achieved. The synthetic utility of this method was demonstrated in the stereoselective synthesis of 4-methylumbelliferyl α-T-antigen.
We also recommend Trading Suppliers and Manufacturers of 4-METHYLUMBELLIFERYL ALPHA-L-RHAMNOPYRANOSIDE (cas 106488-05-5). Pls Click Website Link as below: cas 106488-05-5 suppliers
Prev:An improved method for culturing Streptomyces sahachiroi: Biosynthetic origin of the enol fragment of azinomycin B (cas 106486-76-4)
Next:Overexpression of PEP-19 Suppresses Angiotensin II–Induced Cardiomyocyte Hypertrophy) - 【Back】【Close 】【Print】【Add to favorite 】
-
Health and Chemical more >
-
Related Products
- 4-Methylumbelliferyl 2-amino-2-deoxy-alpha-D-glucopyranoside
- 4-METHYLUMBELLIFERYL ALPHA-L-ARABINOPYRANOSIDE
- 4-Methylumbelliferyl beta-D-cellobioside
- 4-Methylumbelliferyl beta-D-galactoside
- 4-Methylumbelliferyl beta-D-mannopyranoside
- 4-Methylumbelliferyl beta-D-N,N'-diacetylchitobioside
- 4-Methylumbelliferyl beta-D-xylopyranoside
- 4-Methylumbelliferyl butyrate
- 4-Methylumbelliferyl phosphate
- 4-Methylumbelliferyl α-D-mannopyranoside


