The assignment of the 1H and the 13C NMR chemical shifts of N-phenyl-2,4-dimethylbuta-1,3-diene-1,4-sultam
✍ Scribed by R. Radeglia; E. Fanghänel
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 318 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The assignment of the signals in the ^13^C and ^1^H NMR spectra of N‐phenyl‐2,4‐dimethylbuta‐1,3‐diene‐1,4‐sultam is difficult for the signal pairs C‐2 and C‐4, C‐1 and C‐3, (C‐1)H, (C‐2)CH~3~ and (C‐4)CH~3~. The ^13^C NMR spectrum recorded under gated decoupling conditions provide long‐range couplings which make possible an unambiguous assignment of the ^13^C NMR signal pairs. Application of the ^1^H CW off‐resonance decoupling technique in recording the ^13^C NMR spectra enables the assignment information from the ^13^C NMR spectrum to be transferred to the ^1^H NMR spectrum.
📜 SIMILAR VOLUMES
The 1H and 13C NMR resonances of four 3H-naphtho[2,1-b]pyrans were completely and unambiguously assigned by a combination of homonuclear (gs-COSY), 1H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradient-selected correlation experiments.
## Abstract ^1^H and ^13^C NMR data for 13 nitrohistidine derivatives are reported, providing a diagnostic method for the elucidation of the __N__^1^‐(**2**) and the __N__^3^‐substituted (**3**) regioisomers. Spectral assignments of constrained surrogates of His (**4**) and of the His–Gly dipeptide
Three known bisabolane hydrocarbons, a-trans -bergamotene, sesquiphellandrene and zingiberene, were isolated from the aerial parts of Alpinia densibracteata . Their 1H and 13C NMR spectra were completely assigned by using a combination of 13C DEPT and 2D-NMR experiments (1H-1H COSY, single-bond 13C-