Synthesis of four atropdiastereoisomers of C-O-D-O-E ring of vancomycin by sequential cycloetherifications
✍ Scribed by Caroline Vergne; Michèle Bois-Choussy; René Beugelmans; Jieping Zhu
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 236 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
All four aUuixliastereoisomers of model bicyclic C-O-D-O-E ring of vancomycin have been synthesized by way of sequential SNAr based nmcrocyclization.
📜 SIMILAR VOLUMES
## Synthesis of model Iricyclic 1 ) by means of efficient SNAr based cycioetherificalion meOlodology is reported.
Synthesis of a 22-membered macrocycle with an endo aryl-aryl ether linkage and a biaryl bond related to the AB-C-O-D ring of vancomycin is described.
A new approach towards the synthesis of D-O-E-segment of vancomycin by SNAr macrocyclisation is described.