Abstract
We report the reactivity of an electron donor derived from N-methylisatin on reduction by sodium amalgam. Transfer of a clear supernatant solution to iodoarenes affords the products of two-electron reduction. Reductions of sulfones, activated arenesulfonamides, and Weinreb amides are also reported.
| Original language | English |
|---|---|
| Pages (from-to) | 314-322 |
| Number of pages | 9 |
| Journal | Australian Journal of Chemistry |
| Volume | 66 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 7 Jan 2013 |
Keywords
- sulfones
- electron donor
- N-methylisatin
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Dive into the research topics of 'A novel organic electron donor derived from N-methylisatin'. Together they form a unique fingerprint.Projects
- 1 Finished
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Pathways to Impact Award
Littlejohn, D. (Principal Investigator), Cross, A. (Academic), Phelps, A. (Academic) & Ronald, K. (Academic)
EPSRC (Engineering and Physical Sciences Research Council)
1/08/10 → 31/03/11
Project: Research
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