Srikrishna, A and Kumar, Ravi P (2008) Enantiospecific synthesis of (+)-trans-alpha-himachalene via an intramolecular type II carbonyl ene reaction. In: Indian Journal of Chemistry Section B, 47 (9). pp. 1414-1422.
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Abstract
Enantiospecific synthesis of (+)-trans-alpha-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.
| Item Type: | Journal Article |
|---|---|
| Publication: | Indian Journal of Chemistry Section B |
| Publisher: | National Institute of Science Communication and Information Resources |
| Additional Information: | Copyright of this article belongs to National Institute of Science Communication and Information Resources. |
| Keywords: | Enantiospecific synthesis;himachalenes;sesquiterpenes;(R)-carvone;intramolecular ene-reaction. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 18 Nov 2008 10:09 |
| Last Modified: | 18 Nov 2008 10:09 |
| URI: | http://eprints.iisc.ac.in/id/eprint/16444 |
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