Abstract
Reactions of carbohydrate-derived 1,6-enynes under Wacker-like conditions at various dilutions gave rise to the unexpected formation of dimeric tricyclic products. A possible reaction mechanism, in which the importance of specific bond angles is highlighted, is given.
| Original language | English |
|---|---|
| Pages (from-to) | 110-111 |
| Number of pages | 2 |
| Journal | South African Journal of Chemistry |
| Volume | 52 |
| Issue number | 4 |
| Publication status | Published - 1999 |
ASJC Scopus subject areas
- General Chemistry