A stereoselective total synthesis of the novel sesquiterpene kelsoene
โ Scribed by Goverdhan Mehta; K. Srinivas
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 212 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
A total synthesis of cucumin E, a recently isolated triquinane natural product with a new carbon framework, has been achieved. The key step is the flash vacuum pyrolysis (FVP)-induced cyclobutane fragmentation in a readily available pentacyclic caged dione to deliver the triquinane skeleton with fun
Simple and preparatively efficacious lipase-catalysed kinetic resolution of endo, endo-cis-bicyclo[3.3.0]octane-2,6-diol rac-3 has provided ready access to bicyclo[3.3.0]octane-2,6-diones (-)-2 and (+)-2 of high enantiomeric purity. These C 2 -symmetric diones have been further elaborated to the ses