Mehta, Goverdhan and Ramesh, Senaiar S (2004) Enantioselective total synthesis of (+)-panepophenanthrin, a novel inhibitor of the ubiquitin-activating enzyme. In: Tetrahedron Letters, 45 (9). pp. 1985-1987.
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Abstract
An enantioselective total synthesis of the novel natural product (+)-panepophenanthrin has been accomplished in which a biomimetic Diels–Alder dimerisation is a key step. The monomeric precursor 2 was assembled from the readily available Diels–Alder adduct of cyclopentadiene and p-benzoquinone through a short, simple sequence employing chemo- and stereoselective operations.
Item Type: | Journal Article |
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Publication: | Tetrahedron Letters |
Publisher: | Elsevier Science Ltd. |
Additional Information: | Copyright for this article belongs to Elsevier Science Ltd. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 22 Jun 2004 |
Last Modified: | 19 Sep 2010 04:12 |
URI: | http://eprints.iisc.ac.in/id/eprint/412 |
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