Reactions · Wikipedia: Category:Name reactions
Ferrier carbocyclization
Cyclization
Overview
The Ferrier carbocyclization (or Ferrier II reaction) is an organic reaction that was first reported by the carbohydrate chemist Robert J. Ferrier in 1979. It is a metal-mediated rearrangement of enol ether pyrans to cyclohexanones. Typically, this reaction is catalyzed by mercury salts, specifically mercury(II) chloride.
Actions
- This entry doesn't have stoichiometric equivalents on file yet — the Reaction Scale Calculator needs at least one participant tagged with an equivalents value.
- Mechanism / source ↗
- View as JSON ↗
Search literature
More Cyclization reactions
- [3+2]-ANIONIC ELECTROCYCLIZATION USING 2,3-BIS(PHENYLSULFONYL)-1,3-BUTADIENE: trans-4,7,7-TRICARBOMETHOXY-2-PHENYLSULFONYLBICYCLO[3.3.0]OCT-1-ENE (Benzene, 1,1'-[[1,2-bis(methylene)-1,2-ethanediyl]bis(sulfonyl)]bis-) Cyclization
- [3 + 4] ANNULATION USING A [β-(TRIMETHYLSILYL)ACRYLOYL]SILANE AND THE LITHIUM ENOLATE OF AN α,β-UNSATURATED METHYL KETONE: (1R,6S,7S)-4-(tert-BUTYLDIMETHYLSILOXY)-6-(TRIMETHYLSILYL)BICYCLO[5.4.0]UNDEC-4-EN-2-ONE Cyclization
- 5-endo-trig CYCLIZATION OF 1,1-DIFLUORO-1-ALKENES: SYNTHESIS OF 3-BUTYL-2-FLUORO-1-TOSYLINDOLE (1H-Indole, 3-butyl-2-fluoro-1-[(4-methylphenyl)sulfonyl]-) Cyclization
- A GENERAL [3+2] ANNULATION: cis-4-exo-ISOPROPENYL-1,9-DIMETHYL-8-(TRIMETHYLSILYL)BICYCLO[4.3.0]NON-8-EN-2-ONE (4H-Inden-4-one, 1,3a,5,6,7,7a-hexahydro-3,3a-dimethyl-6-(1-methylethenyl)-2-(trimethylsilyl)-, (3aα,6α,7aα)-) Cyclization
- Allan–Robinson reaction Cyclization
- Bergman cyclization Cyclization