| Autor: |
Best, WM, Stick, RV, Tilbrook, DMG |
| Zdroj: |
Australian Journal of Chemistry; 1994, Vol. 47 Issue: 9 p1805-1809, 5p |
| Abstrakt: |
The major products in the controlled benzylation (NaH/PhCH2Cl) of allyl and but-3-enyl β-D-glucopyranosides were the 2,4,6-tri-O-benzyl ethers. Subsequent glycosidations of these tribenzyl ethers gave derivatives of allyl and but-3-enyl β- laminaribioside, the latter being subsequently transformed into 3,4-epoxybutyl β- laminaribioside. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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