Diastereoselective nucleophilic addition to chiral open-chain α-ketoacetals: Synthesis of (R)- and (S)-mevalolactone
- 1 January 1986
- journal article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 27 (19), 2117-2120
- https://doi.org/10.1016/s0040-4039(00)84463-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Diastereoselective addition of grignard reagents to chiral α-ketoacetalsTetrahedron Letters, 1986
- Aymmetric synthesis of (Tetrahedron Letters, 1985
- Non-enzymatic asymmetric synthesis of (R)-(-)- and (S)-(+)-mevalolactone in high enantiomeric purityThe Journal of Organic Chemistry, 1985
- Asymmetric syntheses based on 1,3-oxathianes. 2. Synthesis of chiral tertiary .alpha.-hydroxy aldehydes, .alpha.-hydroxy acids, glycols [R1R2C(OH)CH2OH], and carbinols [R1R2C(OH)Me] in high enantiomeric purity.Journal of the American Chemical Society, 1984
- α-Hydroxylation of ketones using o-iodosylbenzoic acidTetrahedron Letters, 1984
- AN ASYMMETRIC SYNTHESIS OF α-BENZYLOXY ALDEHYDES HAVING A CHIRAL TERTIARY CENTER—AN APPLICATION TO THE ASYMMETRIC SYNTHESIS OF exo-(+)-BREVICOMIN—Chemistry Letters, 1983
- ASYMMETRIC SYNTHESIS OF α-HYDROXY ALDEHYDESChemistry Letters, 1978
- Dimethyl sulfoxide-trifluoroacetic anhydride. New reagent for oxidation of alcohols to carbonylsThe Journal of Organic Chemistry, 1976