Asymmetric Addition of Organometallic Reagents to Homochiral β-Ketoacetals
- 1 September 1988
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 61 (9) , 3380-3382
- https://doi.org/10.1246/bcsj.61.3380
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Chiral acetals in enantio- and diastereoselective substitution or elimination reactionsPure and Applied Chemistry, 1988
- Palladium(II)-catalyzed acetalization of terminal olefins bearing electron-withdrawing substituents with optically active diolsThe Journal of Organic Chemistry, 1987
- Diastereoselective addition of grignard reagents to chiral α-ketoacetalsTetrahedron Letters, 1986
- Additions nucleophiles diastereoselectives sur un monoacetal chiral du glyoxalTetrahedron Letters, 1986
- Diastereoselective nucleophilic addition to chiral open-chain α-ketoacetals: Synthesis of (R)- and (S)-mevalolactoneTetrahedron Letters, 1986
- Asymmetric reduction of ketone reductive cleavage of chiral acetals using organoaluminum reagentsTetrahedron Letters, 1983
- Asymmetric synthesis via acetal templates. 3. On the stereochemistry observed in the cyclization of chiral acetals of polyolefinic aldehydes; formation of optically active homoallylic alcoholsJournal of the American Chemical Society, 1983