## Abstract The dihedral and bond direction angles between all pairs of vicinal protons of the arabinofuranose residue were calculated from the coordinatees of the hydrogen atoms found by an X‐ray study of 3‐__O__‐acetyl‐β‐L‐arabinofuranose 1,2,5‐orthobenzoate. The values found were compared with t
Correlation between the psychotropic potency of cannabinoids and their effect on the 1H-NMR spectra of model membranes
✍ Scribed by Ilana Tamir; Dov Lichtenberg
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 413 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract An earlier paper by the authors has undergone criticism by Jankowski and Rabczenko. The arguments presented are analysed in this paper and the criticism is rejected.
## Abstract The transmission of electronic effects across the ferrocene analogues of chalcones [3‐aryl‐1‐ferrocenyl‐2‐propene‐1‐ones (series 1) and 1‐aryl‐3‐ferrocenyl‐2‐propene‐1‐ones (series 2)], as well as the conformations of both types of ferrocene analogues have been studied. The ferrocene an
## Abstract The complete ^1^H and ^13^C NMR spectral assignments of seven positional isomers of __N__,__N__‐dimethylsulfamoylquinolines 2–8 and quinoline have been made using 1D and 2D NMR techniques, including COSY, HMQC and HMBC experiments. Δδ~H~ and Δδ~C~ substituent effects induced by the sulf
We have developed a family of receptors designed to bind flavin derivatives using specific hydrogen bond interactions. These synthetic host molecules provide a model for specific hvoenzyme-cofactor interactions, allowing isolation and observation of the effects of hydrogen bonding on flavin NMR. We