Synthesis of conjugated dienes from vinyl epoxides, vinyl acetonides and 2,5-dihydrofurans via zirconocene-mediated deoxygenation
The zirconocene-mediated reaction of vinyl epoxides, vinyl acetonides and 2,5-dihydrofurans proceeds via deoxygenation, yielding conjugated dienes.
- Publisher
- ROYAL SOC CHEMISTRY
- Issue Date
- 1997-04
- Language
- English
- Article Type
- Article
- Keywords
DIASTEREOSELECTIVE RING CONTRACTION; DERIVATIVES; COMPLEXES; REDUCTION; ALKYNES
- Citation
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, pp.1095 - 1097
- ISSN
- 0300-922X
- Appears in Collection
- CH-Journal Papers(저널논문)
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