Srikrishna, A and Kumar, Ravi P (2002) Chiral synthons from carvone. Part 53. First enantiospecific synthesis of (-)-9-pupukeanone. In: Tetrahedron Letters, 43 (6). pp. 1109-1111.
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Official URL: http://dx.doi.org/10.1016/S0040-4039(01)02336-X
Abstract
The first enantiospecific total synthesis of (-)-9-pupukeanone, starting from (R)-carvone employing a combination of Michael-Michael reaction and an intramolecular rhodium carbenoid C H insertion reaction as key steps, is described. (C) 2002 Elsevier Science Ltd. All rights reserved.
| Item Type: | Journal Article |
|---|---|
| Publication: | Tetrahedron Letters |
| Publisher: | Elsevier Science |
| Additional Information: | Copyright of this article belongs to Elsevier Science. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 22 Jul 2011 09:52 |
| Last Modified: | 22 Jul 2011 09:52 |
| URI: | http://eprints.iisc.ac.in/id/eprint/39047 |
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