Synthesis and Biological Evaluation of Azido- and Aziridino-hydroxyl-β-lactams Through Stereo- and Regioselective Epoxide Ring Opening.
✍ Scribed by Fides Benfatti; Giuliana Cardillo; Luca Gentilucci; Rossana Perciaccante; Alessandra Tolomelli; Alberico Catapano
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 30 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
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, please click on HTML or PDF.
📜 SIMILAR VOLUMES
## Abstract A variety of hydroxy epoxides have been obtained from well defined hydroxy‐alkenyl derivatives. Their subsequent intramolecular ring‐opening allowed unprecedented classes of spiro‐lactams to be obtained. The effect of the epoxide stereochemistry and of the reaction temperature on the re
## Abstract Efficient methods to prepare β,γ‐disubstituted γ‐lactams with syn and anti configuration are reported.