Continuous Catalytic Synthesis of N- Acetyllactosamine
โ Scribed by Guido F. Herrmann; Dr. Udo Kragl; Prof. Dr. Christian Wandrey
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 279 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The ฮฑ-C-Glycoside of N-acetyllactosamine 8 was synthesised hydroxyl group into an acetamido group by oxidation, oximation, stereoselective reduction and acetylation. Isomeri-from lactose by acetylation, conversion into the allyl ฮฑ-Cglycoside 4, exchanging the protecting groups for benzyl zation of t
A simple and convenient method for the introduction of radiolabel onto C-6' of N-acetyllactosamine is described. 1-N-Benzyl-3-O-beta-D-galactopyranosyl-D-arabinosylamine (1) was synthesized from 3-O-beta-D-galactopyranosyl-D-arabinose as described by Lee and Lee. Compound 1 was oxidized with D-galac