ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone

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] 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 View Item