Diastereoselective addition of grignard reagents to chiral α-ketoacetals
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (1) , 81-82
- https://doi.org/10.1016/s0040-4039(00)83946-5
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Nucleophilic cleavage of acetals using organometallic reagentsJournal of Organometallic Chemistry, 1985
- AN IMPROVED ASYMMETRIC SYNTHESIS OF (R)-(−)-2-ACETYL-5,8-DIMETHOXY-1,2,3,4-TETRAHYDRO-2-NAPHTHOL. A VERSATILE KEY SYNTHETIC INTERMEDIATE OF OPTICALLY ACTIVE ANTHRACYCLINONESChemistry Letters, 1985
- Asymmetric synthesis via acetal templates. 12. Highly diastereoselective coupling reactions with a ketene acetal. An efficient, asymmetric synthesis of R-(+)-α-lipoic acidTetrahedron Letters, 1985
- Stereoselective conjugate addition of organoaluminum reagents to chiral α,β-unsaturated ketalsTetrahedron Letters, 1984
- Asymmetric Synthesis via Acetal Templates. 10. Aldol-Type Reactions. Preparation of a Nonacetic Acid IntermediateJournal of the American Chemical Society, 1984
- Unprecedented regio- and stereochemical control in the addition of organoaluminum reagents to chiral .alpha.,.beta.-unsaturated acetalsJournal of the American Chemical Society, 1984
- Asymmetric synthesis via acetal templates. 6. A stereoselective approach to a key intermediate for the preparation of vitamin D metabolitesJournal of the American Chemical Society, 1984
- Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamideTetrahedron, 1984
- Asymmetric cleavage of chiral acetals by R2CuLi,BF3 reagentsTetrahedron Letters, 1984
- Asymmetric synthesis via chiral acetal templates. 7. Further studies on the cyanation reaction. The use of acetals derived from diols with one chiral centerTetrahedron Letters, 1984