Convenient Synthesis of α,α1-bis(Substituted Furfurylidene) Cycloalkanones and Chalcones Under Microwave Irradiation.
- 1 November 1997
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 27 (21) , 3677-3682
- https://doi.org/10.1080/00397919708007287
Abstract
Condensation of furfural with cycloalkanones and substituted acetophenones catalyzed by solid NaOH results in α, α1-bis (substituted furfurylidene) cycloalkanones and chalcones in high yield under microwave irradiation for a duration of 2 minutes.Keywords
This publication has 14 references indexed in Scilit:
- A Facile Synthesis of α, α'-bis(Substituted Benzylidene)cycloalkanones Catalyzed by bis(p-ethoxyphenyl)telluroxide(bmpto) Under Microwave IrradiationSynthetic Communications, 1997
- Naphthalenes
- Microwave Induced Ferrier RearrangementSynthetic Communications, 1994
- Minute Synthesis of Electrophilic Alkenes under Microwave IrradiationSynthesis, 1994
- APPLICATIONS OF MICROWAVE ENERGY IN ORGANIC CHEMISTRY. A REVIEWOrganic Preparations and Procedures International, 1991
- Synthese organique sous champ microondes : premier exemple d'activation specifique en phase homogeneTetrahedron Letters, 1991
- Preparative scale organic synthesis using a kitchen microwave ovenJournal of the Chemical Society, Chemical Communications, 1990
- Application of commercial microwave ovens to organic synthesis.Tetrahedron Letters, 1986
- The Synthesis of 2,7-Disubstituted Tropones via AromatizationJournal of the American Chemical Society, 1957
- The Partial Hydrogenation of Difurfuralacetone and Related CompoundsJournal of the American Chemical Society, 1950