Srikrishna, A and Satyanarayana, G and Kumar, Pramod (2006) Enantiospecific synthesis of tricyclo5.2.1.0(4,8)]decanes via acid catalysed rearrangement of isotwistanes. In: Tetrahedron Letters, 47 (3). pp. 363-366.
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Official URL: http://dx.doi.org/10.1016/j.tetlet.2005.11.008
Abstract
An acid catalysed rearrangement was employed for the enantiospecific conversion of isotwistanol to tricyclo5.2.1.0(4.8)]-decanes, which provided support for the proposed biosynthesis of allopupukeananes from pupukeananes. The strategy has been further extended to the enantiospecific synthesis of a homobrexane. (c) 2005 Elsevier Ltd. All rights reserved.
| Item Type: | Journal Article |
|---|---|
| Publication: | Tetrahedron Letters |
| Publisher: | Elsevier Science |
| Additional Information: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Molecular rearrangement; Isotwistanes; Pupukeananes; Allopupukeanane. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 20 Oct 2010 05:15 |
| Last Modified: | 20 Oct 2010 05:15 |
| URI: | http://eprints.iisc.ac.in/id/eprint/32872 |
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