The cathodic reductions of two series of substituted quinoxaline di-N-oxides and quinoxalines in acetonitrile were measured in the potential range of 0 to -2.0 V and 0 to -2.3 V us see, respectively. Two irreversible reductions were observed in the first series, and one reversible reduction for the
Cyclic voltammetry of some quinoxaline di-N-oxides and quinoxalines in dimethylformamide
β Scribed by James R. Ames; Melissa A. Houghtaling; Deborah L. Terrian
- Book ID
- 103062557
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 354 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0013-4686
No coin nor oath required. For personal study only.
β¦ Synopsis
The first cathodic reductions of two senes of substituted qumoxahne &-N-oxides and qumoxalmes m dlmethylformamlde were measured The effect of subshtuent on these reductions is reported and reverslhhty IS discussed Key wow3 qumoxalme-N-oxides, qumoxalmes, cychc voltammetry, reverslhhty
π SIMILAR VOLUMES
To gain insight into the mechanism of action, the redox properties of 37 quinoxaline-2-carboxamide 1,4-di-N-oxides with varying degrees of anti-tuberculosis activity were studied in dimethylformamide (DMF) using cyclic voltammetry and first derivative cyclic voltammetry. For all compounds studied, e