𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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


Carbon-13 NMR spectra of heterocycles. S
✍ M. Kausch; H. Dürr; S. H. Doss 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 303 KB

## 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

The 250 MHz 1H NMR spectrum of cinnoline
✍ Giuseppe C. Pappalardo; Salvatore Gruttadauria; Henri Le Bail 📂 Article 📅 1975 🏛 John Wiley and Sons 🌐 English ⚖ 376 KB

## 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 HH couplings have been determined and discussed in relation to theoretical values obtained using INDO calculations.

1H- and 13C-NMR spectra of fenobam
✍ G. Pellizer; F. Rubessa 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 250 KB

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

19F and 1H NMR spectra of halocarbons
✍ Anthony Foris 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 289 KB

## 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

Cyclodimerisation reactions of conjugate
✍ A. De Smet; M. Anteunis 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 English ⚖ 320 KB

## 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

1H NMR and 13C NMR spectra of disulfides
✍ Fillmore Freeman; Christos N. Angeletakis; Tom J. Maricich 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 476 KB

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-&ethylene and benz