Colominic acid (1) is homologous to the weakly immunogenic group B capsular polysaccharide produced by Neisserria meningitidis that causes meningitis in humans [1].
Complete 1H and 13C NMR chemical shift assignments of mono- to tetrasaccharides as basis for NMR chemical shift predictions of oligosaccharides using the computer program CASPER
✍ Scribed by Rönnols, Jerk; Pendrill, Robert; Fontana, Carolina; Hamark, Christoffer; d’Ortoli, Thibault Angles; Engström, Olof; Ståhle, Jonas; Zaccheus, Mona V.; Säwén, Elin; Hahn, Liljan E.; Iqbal, Shahzad; Widmalm, Göran
- Book ID
- 122970257
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 615 KB
- Volume
- 380
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ^1^H and ^13^C NMR chemical shift calculations using the density functional theory–gauge including/invariant atomic orbitals (DFT–GIAO) approximation at the B3LYP/6‐311G++(d,p) level of theory have been used to assign both natural diastereoisomers of 6β‐hydroxyhyoscyamine. The theoretic
Box 13, Cardiff CF1 3XF, UK C-Glycopyranosides and C-glycofuranosides were identilied using 'jC and 'H chemical shift and coupling constant data. Full assignments for all a-and gaoomers were made possible by recourse to carboeproton chemical shift correlation spectroscopy. Greater steric shielding e