Abstract
The Michael-type reaction of quinizarinquinone and 1-ethoxy-1- (trimethylsiloxy)buta-1,3-diene followed by Lewis acid-catalysed [1,5] sigmatropic rearrangement and Friedel-Crafts cyclisation provides a new route to variously functionalized tetracycles.
| Original language | English |
|---|---|
| Pages (from-to) | 102-104 |
| Number of pages | 3 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Dec 1 1987 |
All Science Journal Classification (ASJC) codes
- Molecular Medicine
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Cite this
Hayakawa, K., Aso, M., & Kanematsu, K. (1987). A new approach to linear tetracycles via Michael reactions of quinizarinquinone with O-silylated ketene acetals. Journal of the Chemical Society, Chemical Communications, (2), 102-104. https://doi.org/10.1039/C39870000102