Lewis acid catalysis in micellar systems. Sc(OTf)3-Catalyzed aqueous aldol reactions of silyl enol ethers with aldehydes in the presence of a surfactant
- 1 June 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (26), 4559-4562
- https://doi.org/10.1016/s0040-4039(97)00854-x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Indium trichloride catalysed Mukaiyama aldol reaction in waterChemical Communications, 1996
- 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
- Water-Promoted Organic ReactionsSynthesis, 1994
- Organic reactions in aqueous media - with a focus on carbon-carbon bond formationChemical Reviews, 1993
- Lanthanide Trifluoromethanesulfonates as Reusable Catalysts: Aldol Reactions in Organic SolventsSynthesis, 1993
- Lanthanide Trifluoromethanesulfonates as Stable Lewis Acids in Aqueous Media. Yb(OTf)3 Catalyzed Hydroxymethylation Reaction of Silyl Enol Ethers with Commercial Formaldehyde SolutionChemistry Letters, 1991
- Water-promoted organic reactions: aldol reaction under neutral conditionsThe Journal of Organic Chemistry, 1986
- New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachlorideJournal of the American Chemical Society, 1974
- NEW ALDOL TYPE REACTIONChemistry Letters, 1973