๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Continuous Catalytic Synthesis of N- Acetyllactosamine

โœ 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.


๐Ÿ“œ SIMILAR VOLUMES


Conversion of Lactose into Mimics of N-A
โœ Luigi Lay; Laura Cipolla; Barbara La Ferla; Francesco Peri; Francesco Nicotra ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 275 KB

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

Synthesis of N-acetyllactosamine contain
โœ Nike R. Plessas; Diane A. Blake; Irwin J. Goldstein ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 291 KB

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