Decarboxylation-triggered homo-Nazarov cyclization of cyclic enol carbonates catalyzed by rhenium complex
2021
Decarboxylative homo-Nazarov cyclization catalyzed by a Lewis acid was achieved using a cyclic enol carbonate bearing a cyclopropane moiety as a substrate. Various substrates were converted into the corresponding multi-substituted cyclohexenones in good yields via decarboxylation, followed by 6-membered ring formation involving cyclopropane-ring-opening.
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
47
References
0
Citations
NaN
KQI