Preparation and Oxidative-Chlorination Splitting of Nitro Derivatives OF 1,4-Dithiino[2,3-C:5,6-C′]Diquinoline as a Source of 4-Substituted 5- and 8-Nitro-3-Quinolinesulfonic Acid Derivatives
✍ Scribed by Chrobak, Elwira; Maślankiewicz, Andrzej; Chyćko, Magdalena; Skrzypek, Leszek; Szmielew, Małgorzata; Maślankiewicz, Maria J.; Kusz, Joachim; Zubko, Maciej
- Book ID
- 111945451
- Publisher
- Taylor and Francis Group
- Year
- 2012
- Tongue
- English
- Weight
- 465 KB
- Volume
- 187
- Category
- Article
- ISSN
- 1042-6507
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📜 SIMILAR VOLUMES
Reactions of the title compounds with several nucelophiles suggested that the ring oxygen atom (0-5) accelerated the reactivity of the nitro alkene moiety, but scarcely affected the stereoselectivity of the nucleophilic attack.
## Abstract The ^1^H and ^13^C NMR spectroscopic data for 4‐aryl‐1,4,5,6,7,8‐hexahydro‐2,7,7,5‐oxo‐quinoline 3‐substituted derivatives have been fully assigned by the combination of one‐ and two dimensional experiments (DEPT, HMBC, HMQC, COSY, NOE). Copyright © 2006 John Wiley & Sons, Ltd.