1H- and 13C-n.m.r. assignments and conformational analysis of some monosaccharide and oligosaccharide substrate-analogues of lysozyme
✍ Scribed by Jonathan Boyd; Rod Porteous; Nick Soffe; Muriel Delepierre
- Book ID
- 107725551
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 649 KB
- Volume
- 139
- Category
- Article
- ISSN
- 0008-6215
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📜 SIMILAR VOLUMES
On p. 2515, the following line of copy was inadvertently dropped from between the 15th and 16th lines: In all, 72 possible conformations were considered. The energy minima
## Abstract ^13^C n.m.r. spectra of a series of __N__,__N__‐disubstituted thioamides have been recorded and signal assignments were performed. Separate signals are observed for methylene groups fixed on the nitrogen atom. Since the carbon atom __syn__ to the thiocarbonyl sulfur resonates at higher
## Abstract The ^1^H and ^13^C NMR spectra of D‐amygdalin, a cyanogenetic disaccharide accumulated in food plants, were assigned using a combination of NMR techniques. Methods applied include standard ^1^H–^1^H COSY, proton zero quantum coherence (ZQCOSY), 1D NOE, broad‐band decoupled ^1^H–^13^C ch
Man-(1+6)]-/3-o-Man-OMe, which are structural elements of xylose-containing carbohydrate chains from N-glycoproteins, have been made on the basis of 1D and 2D (DQF 'H-JH COSY, HOHAHA) 500-MHz 'H-n.m.r. spectroscopy and 1D SO-MHz i3C-n.m.r. spectroscopy, respectively. EXPERIMENTAL N.m.r. methods. -N.