Rearrangement of humulene-8,9-epoxide
β Scribed by Ian Bryson; James S Roberts; Abdul Sattar
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- French
- Weight
- 177 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Rearrangement of humulene-6,9-epoxide with tin(IV) chloride leads to the formation of a bicyclic alcohol,the structure of which is related to a rearrangement product of humulene itself.
The three mono-epoxides of humulene ( 1) -( 3) are naturally-occurring'
π SIMILAR VOLUMES
The boron trifluoride catalyzed rearrangement of 7,11-epoxygermacrone (1) provided the new diketone in high yield. This transformation represents the first biomimetic chemical conversion of a germacrane into a humulane skeleton. The cation J\_ is generally considered as the biogenetic precursor of s
Rearrangement of humulene-4,5-epoxide with boron trifluoride etherate leads to the formation of two tricyclic alcohols the structures of which are closely related to that of africanol; the z-ray structure of the E-bromobenzoate of one of the alcohols is reported.
## Abstract For Abstract see ChemInform Abstract in Full Text.