𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H- and 13C-NMR spectroscopy of synthetic monosulfated methyl α-D-mannopyranosides

✍ Scribed by Raphael Ruiz Contreras; Johannis P. Kamerling; Johannes F. G. Vliegenthart


Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
469 KB
Volume
110
Category
Article
ISSN
0165-0513

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Combined 1H, 13C and 11B NMR and mass sp
✍ Reem Smoum; Abraham Rubinstein; Morris Srebnik 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 120 KB

## Abstract Complex formation between __N__‐butylboronic acid and D‐(+)‐glucose, D‐(+)‐mannose, methyl‐α‐D‐glucopyranoside, methyl‐β‐D‐galactopyranoside and methyl α‐D‐mannopyranoside under neutral conditions was investigated by ^1^H, ^13^C and ^11^B NMR spectroscopy and gas chromatography–mass spe

Stereochemical study of hindered α-glyco
✍ Y. Pascal; O. Convert; J. Berthelot; F. Fournier 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 518 KB

Sterically hindered a-glycols, obtained from electrochemical hydrodimenhation of polycyclic ketones (idanone, tetralone, chromanone, flavanone, xanthone and fluorenone), were studied by 'H and -C NMR. Evidence of conformational hindrance was deduced from the 'H spectra; meso or racemic configuration

1H and 13C NMR Spectroscopy analysis of
✍ Lucilia Kato; Raquel Marques Braga 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 52 KB 👁 2 views

A series of acetonides was obtained during the formal synthesis of deoxynojirimycin. The 1 H NMR spectra of these derivatives contain strongly coupled multiplets covering a chemical shift range of about 1 ppm. The spectra are severely complicated by second-order effects and were assigned by 2D NMR a

Total assignment of 1H and 13C NMR spect
✍ P. Ciuffreda; P. Ferraboschi; E. Verza; A. Manzocchi 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 82 KB

## Abstract The complete ^1^H and ^13^C chemical shift assignments of the 13α‐epimer of estrone methyl ether and of estrone methyl ether itself were carried out, making use of one‐ and two‐dimensional NMR techniques (1D HOHAHA, COSY, NOESY, TOCSY and HSQC). Copyright © 2001 John Wiley & Sons, Ltd.