Abstract
Addition of dianions of 3-hydroxybutyrates to benzylideneaniline results in direct formation of trans S*-3-(l-hydroxyethyl)-1,4-diphenyl-2-azetidinone with 95% diastereoselectivity. Inversion of the configuration at Cα, gives the desired trans R*-2-azetidinone in high yield.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3779-3782 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 25 |
| Issue number | 35 |
| DOIs | |
| State | Published - 1984 |
Fingerprint
Dive into the research topics of 'Stereoselective synthesis of 3-(1-Hydroxyethyl)-2-azetidinonesfrom 3-hydroxybutyrates'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS