Abstract
Iodine in the presence of sodium, potassium, and calcium nitrates in acetic acid efficently iodinates activeted arenes and carbazoles. The oxygen was shown not to be an indispensible reaction component. A scheme was suggested describing I+ generation in the system via a series of redox processes with participation of NO- 3.
| Original language | English |
|---|---|
| Pages (from-to) | 1191-1195 |
| Number of pages | 5 |
| Journal | Russian Journal of Organic Chemistry |
| Volume | 35 |
| Issue number | 8 |
| Publication status | Published - Aug 1999 |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
Yusubov, M. S., Perederina, I. A., Filimonov, V. D., Jin, H. W., & Chi, K. W. (1999). Study of a system I2-NO3 in acetic acid as convenient reagent for iodination of arenes and carbazoles. Russian Journal of Organic Chemistry, 35(8), 1191-1195.