Novel 1-Trifluoromethyl Substituted 1,2-Ethylenediamines and Their use for the Synthesis of Fluoroquinolones
โ Scribed by Alexander Ya. Aizikovich; Maxim V. Nikonov; Michael I. Kodess; Vladislav Yu. Korotayev; Valery N. Charushin; Oleg N. Chupakhin
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 97 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
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โฆ Synopsis
A common approach to the synthesis of 1-trifluoromethyl-1,2-ethylenediamines was developed. Based on these original building blocks the new derivatives of N-substituted fluoroquinolones bearing the trifluoromethyl group were obtained. Through-space transmitted coupling constants 7 J F-F between the trifluoromethyl group and F-8 were measured in the 19 F NMR spectra of all fluoroquinolones examined and assigned unequivocally by using 19 F{ 19 F} double resonance technique.
๐ SIMILAR VOLUMES
Use of 1,3-Dipolar Cycloaddition for the Synthesis of Novel Fluoroquinolones. -A novel synthetic way for the modification of 6-fluoroquinoline-4-one-3-carboxylic acids is presented. The 7-azido-derivative (II) undergoes 1,3-dipolar cycloaddition to several alkenes like norbornene, cyclopentenonorbo