Stereoselective hydrolysis of radiolabelled O-pivaloyl derivatives of methyl 2-acetamido-2-deoxy-d-glucopyranoside
✍ Scribed by Srđanka Tomić; Đurđica Ljevaković; Jelka Tomašić
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 442 KB
- Volume
- 188
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The isoquinuclidines **7** and **8** were synthesised and tested as inhibitors of hexosaminidases from jack beans and from bovine kidney. These isoquinuclidines mimick the ^1,4^__B__‐conformer of a __N__‐acetyl‐glucosamine‐derived __β__‐d‐glucopyranoside; they are competitive inhibitors
UDP-D-galactose:fl-D-galactopyranosyl-(l ~ 4)-2-acetamido-2-deoxy-D-glucose a-(1 ~ 3)-Dgalactopyranosyltransferase [E.C . 2.4.1.151] transfers o-galactosyl-residues from the sugar nucleotide with retention of configuration. We report here that synthetic methyl 3'-amino-3'-deoxy-N-acetyllactosaminide