Lewis Acid Catalysis in Aqueous Media: Copper(II)-Catalyzed Aldol and Allylation Reactions in a Water-Ethanol-Toluene Solution
- 1 September 1997
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 26 (9) , 959-960
- https://doi.org/10.1246/cl.1997.959
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Lewis Acid Catalysis of a Diels−Alder Reaction in WaterJournal of the American Chemical Society, 1996
- One-pot Synthesis of β-Amino Esters from Aldehydes Using Lanthanide Triflate as a CatalystTetrahedron Letters, 1995
- Lewis-acid catalysis of a Diels-Alder reaction in waterTetrahedron Letters, 1995
- Repeated Use of the Catalyst in Ln(OTf)3-Catalyzed Aldol and Allylation ReactionsBulletin of the Chemical Society of Japan, 1994
- Lanthanide Triflates as Water-Tolerant Lewis Acids. Activation of Commercial Formaldehyde Solution and Use in the Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous MediaThe Journal of Organic Chemistry, 1994
- Aqueous reactions with a Lewis acid and an organometallic reagent. The scandium trifluoromethanesulfonate-catalyzed allylation reaction of carbonyl compounds with tetraallyltinThe Journal of Organic Chemistry, 1993
- Scandium trifluoromethanesulfonate (Sc(OTf)3). A novel reusable catalyst in the Diels-Alder reactionTetrahedron Letters, 1993
- Lanthanide trifluoromethanesulfonates as reusable catalysts. Michael and Diels-Alder reactionsTetrahedron Letters, 1992
- The Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous MediaTetrahedron Letters, 1992
- Use of lanthanide(III) ions as catalysts for the reactions of amines with nitrilesThe Journal of Organic Chemistry, 1987