Asymmetric glycine enolate aldol reactions: synthesis of cyclosporin's unusual amino acid, MeBmt
โ Scribed by Evans, David A.; Weber, Ann E.
- Book ID
- 111869781
- Publisher
- American Chemical Society
- Year
- 1986
- Tongue
- English
- Weight
- 764 KB
- Volume
- 108
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Introduction. ~ Stereoselective C-C bond forming reactions catalyzed by chiral transition-metal complexes are a topic of fundamental importance [l]. In 1986, Hayashi and Zto reported an elegant asymmetric synthesis of dihydrooxazoles by an efficient gold(1)-catalyzed coupling of aldehydes with 2-iso
Aldol reaetionsof chelatedamino acid esterenolateswith chiral aldehydesgives rise to polyhydroxylated aminoacidain a highlystereoaelective fmhion.Theaeoxygenated aminoacidscanbe convertedinto polyhydroxylatedpipecolinicacids and azaaugarsby cyclizationusingthe Mitaunobu reaction.A interesting epimer