Srikrishna, A and Babu, Ramesh R (2008) Total synthesis of (+/-)-beta-chamigrene and (+/-)-laurencenone C via Ireland ester Claisen rearrangement and an intramolecular type II carbonyl ene reaction sequence. In: Tetrahedron, 64 (46). pp. 10501-10506.
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Abstract
A combination of Ireland ester Claisen rearrangement and intramolecular type II carbonyl ene reactions were exploited for the total synthesis of chamigrenes containing a quaternary carbon atom next to the spirocentre in spiro[5.5]undecane.
| Item Type: | Journal Article |
|---|---|
| Publication: | Tetrahedron |
| Publisher: | Elsevier Science |
| Additional Information: | Copyright of this article belongs to Elsevier Science. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 04 Sep 2009 09:50 |
| Last Modified: | 21 Feb 2019 11:45 |
| URI: | http://eprints.iisc.ac.in/id/eprint/17517 |
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