Lewis acid mediated aldol condensations using thioester silyl ketene acetals
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 42 (3) , 893-909
- https://doi.org/10.1016/s0040-4020(01)87496-2
Abstract
No abstract availableKeywords
This publication has 58 references indexed in Scilit:
- Inept-29Si NMR study of a TiCl4-mediated reaction of an enol silyl etherTetrahedron Letters, 1985
- AN EFFICIENT METHOD FOR THE PREPARATION OF THREO CROSS-ALDOLS FROM SILYL ENOL ETHERS AND ALDEHYDES USING TRITYL PERCHLORATE AS A CATALYSTChemistry Letters, 1985
- Diastereoselectivity in the directed aldol reactions of 1-fluoro-3,3-dimethyl-butanone enolates and enol silyl ethers.Tetrahedron Letters, 1984
- Aldol-additions t0eα- and β-alkoxy aldehydes: The effect of chelation on simple diastereoselectivityTetrahedron, 1984
- Acyclic stereoselection. 27. Simple diastereoselection in the lewis acid mediated reactions of enolsilanes with aldehydes.Tetrahedron Letters, 1984
- Ketene bis(trimethylsilyl) acetals. Cross-aldol condensation with aldehydes. Stereochemistry of the reactionTetrahedron Letters, 1984
- Acyclic stereoselection. 16. High diastereofacial selectivity in Lewis acid mediated additions of enol silanes to chiral aldehydesJournal of the American Chemical Society, 1983
- Stereoselection in the condensation between ethyl propionate and aldehydesTetrahedron Letters, 1979
- 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