A comparative study of NMR chemical shifts of sparteine thiolactams and lactams
✍ Scribed by Renata Kolanoś; Waleria Wysocka; Tadeusz Brukwicki
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 146 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
The 13 C and 1 H NMR spectra of the four possible thiolactams of sparteine (1) were recorded and the thiolactam group effects were determined. Most of the effects are greater than those of the lactam group in the oxo analogs. A good linear correlation between the 13 C chemical shifts of CvS and those of CvO was found. The effects could help in assignment of the spectra and determination of conformation of thiolactams and related thiocarbonyl compounds.
📜 SIMILAR VOLUMES
## Abstract The ^15^N NMR spectra of three __N__‐alkyl‐δ‐carbomethoxyvalerothiohydroxamic acids (**2**) and six synthesized __N__‐isopropylbenzothiohydroxamic acids (**3**) were measured and compared with appropriate spectra of structurally similar hydroxylamines (**1**), benzohydroxamic acids (**4
## Abstract The ^1^H NMR 270‐MHz spectra of substituted 2‐phenylthiazolidines were recorded and the substituent‐induced chemical shifts (SCS) of the benzylic proton plotted against σ, the correlation coefficient being 0.801 and −ρ = 10.29 Hz. Halogens show deviations in the SCS plots. When the halo