Synthesis, 15N NMR spectra and GIAO calculated data of the seven positional isomers of 15N-labeled N,N-dimethylsulfamoylquinoline
✍ Scribed by Krzysztof Marciniec; Andrzej Maślankiewicz; Maria J. Maślankiewicz; Rafał Kurczab
- Book ID
- 113806281
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 262 KB
- Volume
- 1015
- Category
- Article
- ISSN
- 0022-2860
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
4-15N-2,3,5-Trimethylpyrazine (A) was synthesized by dechlorination of 4-15N-6-chloro-2,3,5-trimethylpyrazine (I), the key intermediate, derived from 15N-D~alanine (a). 1-15N-2, 3,5-Trimethylpyrazine (2) was prepared by decarboxylation of 1-15N-2,3,5-trimethyl-pyrazine-6- carboxylic acid (10) obtai
## Abstract ^13^C NMR spectra of four types of azo coupling products from benzenediazonium chloride have been measured and interpreted, viz. hydrazo compounds with an intramolecular hydrogen bond (3‐methyl‐1‐phenylpyrazole‐4,5‐dione 4‐phenylhydrazone), azo compounds without an intramolecular hydrog