## Abstract The ^13^C NMR spectra of 1,3‐propanesultam, 2,4‐butanesultam, 1,4‐butanesultam, 1,3‐propanesultone and 1,4‐butanesultone, as well as some of their unsaturated analogs 2,4‐dimethylbuta‐1,3‐diene‐1,4‐sultone and 2,4‐dimethylbuta‐1,3‐diene‐1,4‐sultam, have been recorded. The observed chemi
60, 90 and 250 MHz 1H NMR spectra of sultams and sultones
✍ Scribed by K.-H. Albert; H. Dürr; S. H. Doss; J. P. Zahra
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 370 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The high‐field ^1^H NMR spectra of 1,3‐propanesultams (2), 2,4‐butanesultams (3) and 2,4‐dimethyl‐1,3‐butadienesultams (6) are reported. Comparison of 2,3 and 6 with 1,3‐propanesultone (1) and 2,4‐dimethyl‐1,3‐butadienesultone (5) reveals that the paramagnetic shift induced by the NH group is smaller than that induced by oxygen. NMR spectra at lower temperature show coupling effects with the NH proton. A half‐chair conformation was deduced for 2,4‐butanesultam from coupling constants and from a conformational analysis based on the R values, but a chair‐chair interconversion could not be detected in the temperature range between 210 and 330 K. An unambiguous assignment was carried out for the methyl signals in the spectrum of 5 by homodecoupling experiments.
📜 SIMILAR VOLUMES
## Abstract The proton NMR spectrum of cinnoline has been measured at high field (250 MHz) and analysed as an H‐8‐de‐coupled ABCXY and H‐4‐decoupled ABCX system. Inter‐ring HH couplings have been determined and discussed in relation to theoretical values obtained using INDO calculations.
0 'H-and 'W-NMR data and spectral assignments are reported for fenobam using noise modulated gated, single frequency off resonance, and single frequency selective proton decoupling techniques. Keyphrases 0 Fenobam-'H-and 13C-NMR spectroscopic analysis 0 'H-and 'T-NMR spectroscopy-analysis of fenoba
## Abstract ^19^F NMR chemical shifts and coupling constants are reported for 215 compounds. For 77 of these compounds, ^1^H NMR spectral data are also given. Long‐range couplings, including ^8^J(F,F) and ^5^J(F,H), are reported. The complexity of halocarbon spectra owing to the presence of rotatio
## Abstract The palladium catalysed reaction of butadiene with aldehydes yields 2‐substituted 3,6‐divinyl‐tetrahydropyrans.^1–4^ The reaction has been extended to isoprene and myrcene. With formaldehyde only 2,5‐substituted pyrans have been isolated. The isomeric tetrahydropyrans obtained were full
The 'H NMR and 13C NMR spectra of neopentyl and benzyl substituted disulfides, thiosulfinates, thiosulfonates, thiols, sulfides, sulfinic acids and sulfonic acids are reported. The deshielding electron withdrawing effects of -SO, -SO,, -SOz-, -SO,H, -SO,-, S 0 , H and S03CH3 on or-ðylene and benz