Srikrishna, Adusumilli and Pardeshi, Vijendra H and Mahesh, Konda (2010) Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone. In: Tetrahedron: Asymmetry, 21 (20). pp. 2512-2516.
![[img]](http://eprints.iisc.ernet.in/style/images/fileicons/application_pdf.png) |
PDF
Total.pdf - Published Version Restricted to Registered users only Download (417Kb) | Request a copy |
Official URL: http://dx.doi.org/10.1016/j.tetasy.2010.09.008
Abstract
The enantiospecific total synthesis of two epimers of the sesquiterpene isocalamusenone has been accomplished starting from the readily available monoterpene (R)-limonene which of the natural product established the stereostructure and the absolute configuration (C) 2010 Elsevier Ltd All rights reserved
| Item Type: | Journal Article |
|---|---|
| Additional Information: | Copyright of this article belongs to Elsevier Science. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 07 Feb 2011 10:33 |
| Last Modified: | 07 Feb 2011 10:33 |
| URI: | http://eprints.iisc.ernet.in/id/eprint/35006 |
Actions (login required)
 |
View Item |
