𝔖 Bobbio Scriptorium
✦   LIBER   ✦

13C and 17O NMR of some substituted oxiranes. Chemical shifts and quantitative correlations

✍ Scribed by J. P. Monti; R. Faure; A. Sauleau; J. Sauleau

Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
539 KB
Volume
24
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

1H and 13C NMR chemical shifts of some t
1H and 13C NMR chemical shifts of some thienyl-substituted chromenes
✍ C. Moustrou; N. Rebiere; M. Frigoli; E. Pottier; R. Guglielmetti; R. Faure πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 172 KB πŸ‘ 2 views

The complete assignment of the 1H and 13C NMR spectra of eight thienyl-substituted chromenes was achieved by the concerted application of homonuclear (gs-COSY), 1H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradientselected correlation experiments.

Application of 17O Chemical Shift Substi
Application of 17O Chemical Shift Substitution Parameters to D-Hexopyranoses. Correlation between the 17O and 13C Chemical Shifts at the Anomeric Centre
✍ J. Schulte; J. Lauterwein πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 473 KB πŸ‘ 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

17O NMR of nucleosides. 3β€”Chemical shift
17O NMR of nucleosides. 3β€”Chemical shifts of substituted uridines and ribothymidines
✍ Herbert M. Schwartz; Malcolm Maccoss; Steven S. Danyluk πŸ“‚ Article πŸ“… 1985 πŸ› John Wiley and Sons 🌐 English βš– 886 KB

Uridine and ribothymidine derivatives, bearing different substituents at C-5 and enriched (Cu 50%) with 1 7 0 in the 0-4 and 0-2 carbonyls, have been studied via "0 NMR in both acetonitrile and aqueous solvents. The solvent shift differences between acetonitrile and water at 0-4 (30-42ppm) and 0-2 (

Microcomputer prediction and assessment
Microcomputer prediction and assessment of substituted benzene 13C NMR chemical shifts
✍ Richard Angus Hearmon; Hok-Ming Liu; Simon Laverick; Paul Tayler πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 496 KB πŸ‘ 1 views

## Abstract A ^13^C NMR chemical shift prediction and spectral assessment program was written in Turbo Prolog. Based on the large data compendium of Ewing it allows the rapid assessment of the spectral–structural relationship for substituted benzene rings.