𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Chemical shift anisotropy of the anomeric protons in α- and β-D-glucose

✍ Scribed by Leszek Poppe; Herman van Halbeek


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
385 KB
Volume
31
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Values for the chemical shift anisotropies of the α‐ and β‐anomeric protons in [1‐^13^C]‐D‐glucose were measured by ortho‐ROESY and SLOESY experiments using non‐selective and selective ^1^H spin‐locking by DANTE pulse trains, respectively. The experiments were performed under the condition ω~H~τ~o~ ≈ 1, in order to enhance cross‐correlated cross‐relaxation due to interference between ^1^H chemical shift anisotropy and ^1^H‐^13^C dipolar interactions. Assuming axial symmetry for the ^1^H chemical shift tensor, chemical shift anisotropy values of Δσ~H‐1(α)~ ≈ −6.1 ppm and Δσ~H‐1(β)~ ≈ −2.4 ppm were obtained.


📜 SIMILAR VOLUMES


Chemical shift non-equivalence of ring p
✍ A. Vigevani; B. Gioia; G. G. Gallo 📂 Article 📅 1970 🏛 John Wiley and Sons 🌐 English ⚖ 216 KB

## Abstract A study is reported on the chemical shift non‐equivalence of the diastereotopic protons at C‐4 in identically 3,3‐disubstituted β‐lactams having an asymmetric carbon atom in positions ranging from β to ε of the chain attached to the nitrogen atom. The non‐equivalence has been correlated

Proton chemical shifts in NMR: Part 17.
✍ Raymond J. Abraham; Marcos Canton; Lee Griffiths 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 188 KB

## Abstract The ^1^H NMR spectra of a number of alkenes of known geometry were recorded in CDCl~3~ solution and assigned, namely ethylene, propene, 4‐methylcyclohexene, 1,4‐dimethylcyclohexene, methylene cyclohexane (in CFCl~3~–CD~2~Cl~2~ at 153 K), 5‐methylene‐2‐norbornene, camphene, bicyclopentad

Application of 17O Chemical Shift Substi
✍ J. Schulte; J. Lauterwein 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 473 KB 👁 2 views

1 7 0 chemical shift substitution parameters obtained previously from the investigation of the conformationally rigid 1,6-anhydro-/?-~-hexopyranoses were applied to five a,/?-D-hexopyranoses: allose, glucose, mannose, gulose and galactose. The "0 chemical shifts predicted for the endocyclic ether ox