Alumina-promoted fast solid-phase Michael addition of enamines with conjugated enones under microwave irradiation
- 1 January 2002
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 43 (1) , 143-145
- https://doi.org/10.1016/s0040-4039(01)02049-4
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Catalysis of the Michael Reaction and the Vinylogous Michael Reaction by Ferric Chloride HexahydrateSynlett, 2001
- Synergy between Heterogeneous Catalysis and Microwave Irradiation in an Efficient One-Pot Synthesis of Benzene Derivatives via Ring-Opening of Diels-Alder Cycloadducts of Substituted FuransSynlett, 2001
- The Double Annulation of Tethered Diacids and Alkynones: History and ScopeSynlett, 2001
- Studies on the reactions of α,β-enones with allyl indium reagent; effects of TMSCl as promoter on regioselectivityTetrahedron Letters, 2001
- Annulation routes to trans-decalinsTetrahedron, 1999
- Our Recent Contribution to the Field of Anionic Domino TransformationsSynlett, 1999
- Trifluoromethanesulfonic Acid, an Unusually Powerful Catalyst for the Michael Addition Reaction of β-Ketoesters under Solvent-Free ConditionsThe Journal of Organic Chemistry, 1999
- Iron(iii) catalysis of the Michael reaction of 1,3-dicarbonyl compounds and enonesChemical Communications, 1997
- Novel chemoselective and diastereoselective iron(III)-catalysed Michael reactions of 1,3-dicarbonyl compounds and enonesJournal of the Chemical Society, Perkin Transactions 1, 1997
- The First Heterobimetallic Multifunctional Asymmetric CatalystJournal of the American Chemical Society, 1995