Proton and carbon-13 NMR studies of methyl-(6-O-L-phenylalanyl)-α-D-glucoside and methyl-(6-O-D-phenylalanyl)-α-D-glucoside by 1H and 13C nmr showed that the LD compound is more flexible than DD and that DD probably assumes a folded conformation.

✍ Scribed by Siu-Leung Lee; Wei-Jun Zhang; Michael McLauglin; Pamela Roberts

• Publisher: Elsevier Science
• Year: 1982
• Tongue: French
• Weight: 266 KB
• Volume: 23
• Category: Article
• ISSN: 0040-4039
• DOI: 10.1016/s0040-4039(00)87317-7