## Abstract The conformational state of the [3.3.3]propellane framework for 14‐hydroxymodhephene was determined by extensive application of one‐ and two‐dimensional ^1^H and ^13^C NMR spectroscopy combined with x‐ray diffraction studies of a synthesized derivative, spectral simulation and molecular
1H NMR model studies of amphotericin B: Comparison of x-ray and NMR stereochemical data
✍ Scribed by Pawel Sowiński; Jan Pawlak; Edward Borowski; Pierluigi Gariboldi
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 407 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^1^H NMR data for amphotericin B methoxycarbonylmethylamide extracted from DQF‐COSY, ROESY and 1D spectra were compared with x‐ray data for amphotericin B. The conformation of amphotericin B in solution was identical with that found by x‐ray analysis in the solid state. Most of the relay artifacts observed in the ROESY spectrum were recognized, and their pathways of formation were assigned.
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Sterically hindered a-glycols, obtained from electrochemical hydrodimenhation of polycyclic ketones (idanone, tetralone, chromanone, flavanone, xanthone and fluorenone), were studied by 'H and -C NMR. Evidence of conformational hindrance was deduced from the 'H spectra; meso or racemic configuration
## Abstract The synthesis and NMR spectra of the __N__‐borane adducts of two diimines, __N__‐borane‐bis(α‐phenylethylidene)ethylenediamine and __N__‐borane‐bis(α‐phenylbenzylidene)ethylenediamine, and four imines, __N__‐borane‐α‐methylethylidene‐2‐phenylethylamine, two __N__‐borane‐α‐phenylethylide