Synthesis of allyl and benzyl β-d-glucopyranosides, and allyl β-d-galactopyranoside from d-glucose or d-galactose and the corresponding alcohol using almond β-d-glucosidase
✍ Scribed by Gabin Vic; David H.G. Crout
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 333 KB
- Volume
- 279
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A number of homologous (R)-and (S)-1-methoxyalkyl ## P-D-glUCO- pyranosides, carrying at the wend of the C,\_, atom alkyl chain either an azido-or an amino group, were used as substrates or competitive inhibitors of p-D-glucosidase from sweet almond emulsin. All azides were cleaved at comparative
## 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
D-Ribose was converted into methyl 5-O-benzyl-beta-D-ribofuranoside and this, on tin-mediated allylation, gave a mixture of the 2-O-allyl and 3-O-allyl derivatives which were separated by chromatography. The more polar isomer was characterised as the 3-O-allyl derivative after conversion via 3-O-all