Lewis acid promoted aldol additions of α-thiosilylketeneacetals to α-alkoxy aldehydes: diastereoselective synthesis of -α-methylene-β-hydroxy-∂-alkoxy esters.
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (52) , 6509-6512
- https://doi.org/10.1016/s0040-4039(00)99039-7
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Lewis acid mediated 1,2-asymmetric lk-induction to α-alkoxyaldehyde: synthesis of α-nonsubstituted β, γ-syn-dihydroxyketone and esterTetrahedron Letters, 1985
- Acyclic stereoselection. 28. Use of stereoselective aldol methodology in the total synthesis of cladinose.Tetrahedron Letters, 1985
- Stereoselective aldol additions to α-alkoxy aldehydes using thioester silyl ketene acetals,Tetrahedron Letters, 1985
- Acyclic stereoselection. 32. Synthesis and characterization of the diastereomeric (4S)-pentane-1,2,3,4-tetraolsThe Journal of Organic Chemistry, 1985
- High diastereoface selection in an ester enolate addition to .alpha.-alkoxy aldehydes: stereoselective synthesis of .alpha.-methylene-.beta.-hydroxy-.gamma.-alkoxy estersThe Journal of Organic Chemistry, 1984
- Chelation or Non‐Chelation Control in Addition Reactions of Chiral α‐ and β‐ Alkoxy Carbonyl Compounds [New Synthetic Methods (44)]Angewandte Chemie International Edition in English, 1984
- A 13C and 1H NMR study of diastereomeric α‐methylidene‐β‐hydroxy‐γ‐alkoxy estersMagnetic Resonance in Chemistry, 1984
- Aldol-additions t0eα- and β-alkoxy aldehydes: The effect of chelation on simple diastereoselectivityTetrahedron, 1984
- Allergenic .alpha.-methylene-.gamma.-butyrolactones. .beta.-Hydroxy-.alpha.-methylene-.gamma.-butyrolactones. 2. Syntheses from ethyl 2-(phenylthio)propionate and .alpha.-acetoxy aldehydesThe Journal of Organic Chemistry, 1983
- Stereoselective synthesis of α-methylene-β-hydroxy-γ-alkoxy esters from α-alkoxy aldehydesJournal of the Chemical Society, Chemical Communications, 1983