SURFACE-MEDIATED SOLID-PHASE REACTION .6. MUKAIYAMA-MICHAEL ADDITION OF SILYL ENOL ETHERS TO ALKYL VINYL KETONES ON THE SURFACE OF ALUMINA - A SIMPLE AND CONVENIENT METHOD FOR THE SYNTHESIS OF 1,5-DIKETONES

Authors
RANU BC SAHA M BHAR S
Citation
Bc. Ranu et al., SURFACE-MEDIATED SOLID-PHASE REACTION .6. MUKAIYAMA-MICHAEL ADDITION OF SILYL ENOL ETHERS TO ALKYL VINYL KETONES ON THE SURFACE OF ALUMINA - A SIMPLE AND CONVENIENT METHOD FOR THE SYNTHESIS OF 1,5-DIKETONES, Journal of the Chemical Society. Perkin transactions. I, (15), 1994, pp. 2197-2199
Citations number
60
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
15
Year of publication
1994
Pages
2197 - 2199
Database
ISI
SICI code
0300-922X(1994):15<2197:SSR.MA>2.0.ZU;2-P
Abstract
Michael addition of silyl enol and dienol ethers to alkyl vinyl ketone s occurs in high yield through a simple solvent-free reaction on the s urface of anhydrous zinc chloride-impregnated alumina to give 1,5-dike tones.