Chiral Acylsilanes in Organic Synthesis. Part 2. The role of the solvent, the organometallic reagent, and the nature of the substrate for the diastereoselectivity of 1,2‐additions to racemic alkoxymethyl‐substituted acylsilanes
- 11 August 1993
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 76 (5) , 1876-1889
- https://doi.org/10.1002/hlca.19930760507
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Chiral Acylsilanes in Organic Synthesis. Diastereoselective 1,2‐Additions to Racemic Alkoxymethyl‐Substituted AcylsilanesHelvetica Chimica Acta, 1991
- OrganometallchemiePublished by Springer Nature ,1988
- Diastereoselective addition of grignard reagents to chiral α-ketoacetalsTetrahedron Letters, 1986
- Solvent effects on chemical reactivity. Evaluation of anion- and cation-solvation componentsJournal of the American Chemical Society, 1983
- Synthesis of α-Silyl Ketones via 1,3-DithianesJournal of the American Chemical Society, 1967
- Synthesis of Silyl and Germyl KetonesJournal of the American Chemical Society, 1967
- Comparison of the Reactions of Grignard Reagents and Dialkylmagnesium Compounds in Addition, Reduction, and Enolization Reactions1The Journal of Organic Chemistry, 1962
- Studies in Stereochemistry. XXX. Models for Steric Control of Asymmetric Induction1Journal of the American Chemical Society, 1959
- The Protonation of the Carbonyl Group. I. The Basicity of Substituted Acetophenones1Journal of the American Chemical Society, 1958
- Single Ion Free Energies and Entropies of Aqueous IonsThe Journal of Chemical Physics, 1955