## Abstract Structural studies in the solid state by X‐ray crystallography and by ^13^C and ^15^N CPMAS NMR spectroscopy carried out on a series of 2‐aminotroponimine derivatives **2**−**5** has allowed to establish the existence of hydrogen bonding and to determine the most stable tautomer. Almost
The structure of glycosyl amides: A combined study by NMR spectroscopy, X-ray crystallography, and computational chemistry
✍ Scribed by Martín Avalos; Reyes Babiano; María J. Carretero; Pedro Cintas; Francisco J. Higes; JoséL. Jiménez; Juan C. Palacios
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 799 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
The structure of N-formyl, N-acetyI-N-methyl, and N-acetyl glycosylamines has been studied by NMR spectroscopy in solution, single crystal X-ray diffractometry, and corroborated by PM3 semiempirical calculations. The results quite agree with an anti conformation around the glycosydic bond for these substances.
📜 SIMILAR VOLUMES
## Abstract 1‐Hydroxymethylindazole and 1‐hydroxymethylbenzotriazole have been studied in solution by ^1^H, ^13^C and ^15^N NMR spectroscopy and the X‐ray structure of the second compound determined. DFT and GIAO calculations have been used to discuss geometries, energies (comparatively with 2‐subs