Abstract
Valerophenones containing a substituent at alpha position to the carbonyl group show the remarkable substituent effects on their photochemical reactions. α-Bromovalerophenone gives only the C-Br bond cleavage products, but the α-chlorovalerophenone follows the classical Norrish/Yang reaction pathway predominantly.
| Original language | English |
|---|---|
| Pages (from-to) | 42-44 |
| Number of pages | 3 |
| Journal | Bulletin of the Korean Chemical Society |
| Volume | 25 |
| Issue number | 1 |
| DOIs | |
| State | Published - 20 Jan 2004 |
Keywords
- Halo ketone
- Photochemistry
- Substituent effect
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