Two new photoaffinity reagents having photoreactive groups attached to C-6 of D-galactose have been prepared. 6-N-(6Azido-2-hydroxybenzoyl)-D-glucopyranosylamine and 6-N-(4-azido-2-hydroxybenzoyl)-D-galactopyranosylamine were synthesized by acylation of the protected amino sugars with 4-azidosalicoy
Synthesis and growth regulator activity of fatty acyl derivatives of d-glucose and d-galactose
✍ Scribed by James N. Bemiller; George L.-Y. Leung; John E. Yopp
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 659 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0031-9422
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract Sugar–iminosugar hybrid molecules made up of D‐glucose and D‐galactose with pyrrolidine‐based iminosugars, viz. 1,4‐dideoxy‐1,4‐imino‐L‐xylitol and 1,4‐dideoxy‐1,4‐imino‐L‐lyxitol, are synthesized from glycal epoxides and found to be moderate glycosidase inhibitors. (© Wiley‐VCH Verlag
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract L‐Glucose derivatives are prepared by two different routes. The first involves a modification of the previously reported multi‐step approach by __Shiozaki__^8^, starting from a D‐glucurono‐1,5‐lactone derivative, resulting in the isolation of 2,3,4,6‐tetra‐__O__‐benzyl‐L‐glucopyranose.