13C Chemical shifts and conformational equilibria in quaternary piperidinium salts
✍ Scribed by Makiko Sugiura; Narao Takao
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 250 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Carbon‐13 nuclear magnetic resonance spectra of a series of N‐methyl‐N‐alkylpiperidinium salts have been measured, and the observed chemical shifts analysed in terms of the stereochemical and conformational properties of the molecules. Furthermore, the differences of the free energy (Δ__G__°) between two conformers on ring inversion have been estimated.
📜 SIMILAR VOLUMES
## Abstract ^13^C‐nmr chemical shifts of backbone carbonyl and side‐chain β‐carbons in polypeptides provide structural information. Recent utilization of substituent effects on ^13^C‐nmr chemical shifts (principally γ‐effects) has permitted the rationalization of their sequence and conformation dep
## Abstract The ^13^C NMR chemical shifts of the α‐carbon atoms in cations [NR~4~]^+^, [NR~3~CH~2~Ph]^+^ and [PR~4~]^+^ [R = Me, Et, Pr^__n__^, Bu^__n__^ or Pe^__n__^ (__n__‐pentyl)] are found at anomalously high field in comparison with the corresponding shifts in RCl or RNH~2~. This is ascribed i
The 13C chemical shifts of 2-R-3-methylbenzothiazolium quaternary salts and the corresponding ZRbenzothiazoles are presented. ## KEY WORDS I3C NMR Substituent effects 2-R-3-methylbenzothiazoliurn quaternary salts 2-R-benzothiazoles reveal some systematic trends in the 13C data for these comr>ound
Cross-polarization magic-angle spinning solid-state NMR spectroscopy has been used to investigate the dependence of 13 C sugar chemical shifts on specific conformational parameters of a variety of ribonucleotides and ribonucleosides. Solid-state NMR is a valuable tool for nucleoside and nucleotide s