𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The influence of methylation on 13C chemical shifts of galactose derivatives

✍ Scribed by W. Voelter; E. Breitmaier; E.B. Rathbone; M. Stephen

Publisher
Elsevier Science
Year
1973
Tongue
French
Weight
214 KB
Volume
29
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

13C NMR chemical shifts of N-unsubstitut
13C NMR chemical shifts of N-unsubstituted- and N-methyl-pyrazole derivatives
✍ Pilar Cabildo; Rosa Maria Claramunt; Jose Elguero πŸ“‚ Article πŸ“… 1984 πŸ› John Wiley and Sons 🌐 English βš– 331 KB

## Reference Data 13C NMR Chemical Shifts of N u nsubstituted-and N-MethyI-Pyramle Derivatives 13C shielding data for 100 derivatives of pyrazole are reported. These include methyl, ethyl, n-propyl, tert-butyl, phenyl, hydroxymethyl, carboxyl, ethoxycarbonyl, cyano. amino, hydrazino, nitro, azido,

The effect of ring strain on 13C chemica
The effect of ring strain on 13C chemical shifts
✍ Kenneth R. Gooding; W.Roy Jackson; Christopher F. Pincombe; Douglas Rash πŸ“‚ Article πŸ“… 1979 πŸ› Elsevier Science 🌐 French βš– 119 KB

It has been well established that the 13 C chemical shift of ring carbon atoms normally moves to higher field with decreasing ring size both for carbocyclic 1 and saturated heterocyclic2 compounds. Recent work3 has shown that in compounds where two of the cyclo-

13C chemical shifts and conformational a
13C chemical shifts and conformational analysis of methyl substituted thiacyclopentanes
✍ G. Barbarella; P. Dembech πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 English βš– 530 KB

## Abstract The ^13^C NMR spectra of thiacyclopentane (thiolane) and its mono‐ and dimethyl derivatives at positions other than the heteroatom are reported. The ^13^C shieldings are found to be consistent with a description of these compounds in terms of equilibria between half‐chair conformers. An