Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/2003| Title: | Enantiospecific synthesis of (+)-trans-⍺-himachalene via an intramolecular type II carbonyl ene reaction |
| Authors: | Srikrishna, A Kumar, P Ravi |
| Keywords: | Enantiospecific synthesis;Himachalenes;Sesquiterpenes;(R)-carvone;Intramolecular ene-reaction |
| Issue Date: | Sep-2008 |
| Publisher: | CSIR |
| Abstract: | Enantiospecific synthesis of (+)-trans-⍺-himachalene starting from (R)-carvone is described. An intramolecular type II carbonyl ene reaction has been employed as the key step for the construction of the bicyclo[5.4.0]undecane ring system. |
| Page(s): | 1414-1422 |
| ISSN: | 0376-4699 |
| Appears in Collections: | IJC-B Vol.47B(09) [September 2008] |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 47(9) 1414-1422.pdf | 134.46 kB | Adobe PDF | View/Open |
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