Enantiopure α-hydroxy-β-lactams via stereoselective glycosylation
✍ Scribed by Bimal K. Banik; Maghar S. Manhas; Ajay K. Bose
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 207 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A diastereoselective synthesis of [5-Lactams 5a-e and 6a-e has been achieved, via a Staudinger reaction using imines derived from (1S)-(+)-camphor-10-sulfonamide, in good yields. The major diastereomers 6a-e were isolated in pure form by crystallization. The absolute configuration of the [5-1actam 6
A convement and raprd synthesis of enantiopure (I -hydroxy-$ -lactams using microwave-induced organic reaction enhancement chemistry has been developed. Reactions in domestic microwave ovens, which are very convenient and economical for small scale work in research or teachmg laboratories, can also
Both threo-and erythro-8-hydroxy-u-methylcarboxylic acid thiol esters are stereoselectively synthesized through an aldol-type condensation of vinyloxyboranes derived formally from S-tertbutyl propanethioate. The basic carbon skeletons of many macrolide antibiotics are biosynthesized through a serie