A Practical Total Synthesis of (+)-Spirolaxine Methyl Ether
โ Scribed by Yadav, J. S.; Sreenivas, M.; Srinivas Reddy, A.; Subba Reddy, B. V.
- Book ID
- 125426446
- Publisher
- American Chemical Society
- Year
- 2010
- Tongue
- English
- Weight
- 786 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ 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.
An efficient reductive methylation of the tricyclic ketone 12 in anhydrous ammonia provided the 8 ,y-unsaturated ketone 15 in high yield which was subsequently converted into (i)-shonanyl methyl ether 12) and (+I-ferruginylmethyl ether (5). Shonanol, a tricyclic diterpene, was isolated from Liboced