Regioselective Carbomethoxylation of Chiral Epoxides: A New Route to Enantiomerically Pure β-Hydroxy Esters
✍ Scribed by Hinterding, Klaus; Jacobsen, Eric N.
- Book ID
- 126503890
- Publisher
- American Chemical Society
- Year
- 1999
- Tongue
- English
- Weight
- 92 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Successive treatment of chiral esters J\_ with LDA/Me3SiCl and NBS or NCS gave crystalline a-haloesters 2 which furnished halohydrins 4 and terminal epoxides 2 in high e.e.. The practical, chiral auxiliaries Xa and Xb (Scheme 1) confer high II-face differentiation to Diels-Alder-l and organocopper a
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v