Efficient synthesis of 16–28 membered macrocyclic crown amides via ring closing metathesis
✍ Scribed by Yehia A Ibrahim; Haider Behbehani; Maher R Ibrahim; Rana N Malhas
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 224 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
Ring closing metathesis of suitable diamides containing 1,v-dienes led to efficient synthetic approaches towards macrocylic polyoxadiamides 1 -18 with 16 -28 membered ring sizes in good to excellent yields using Grubbs' catalyst.
📜 SIMILAR VOLUMES
## 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.
RCM of suitable diamides containing 1,v-dienes led to efficient atom economic synthetic approaches towards macrocylic polyoxadiamides with 15-25-membered ring sizes.
RCM of suitable ␣,-dienes led to efficient atom economic synthetic approaches towards azacrown ether derivatives with 8-40 membered ring sizes.