Alpha-hydroxy cyclopentenones from alpha-diketones
- PMID: 15957943
- DOI: 10.1021/ol050970x
Alpha-hydroxy cyclopentenones from alpha-diketones
Abstract
[reaction: see text] Metalloenolates derived from alpha,beta-unsaturated alpha-diketones undergo cyclization to alpha-hydroxy cyclopentenones. This is apparently the first reported Nazarov reaction that takes place in the presence of base.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources