Enantiospecific approach to the tricyclic core structure of tricycloillicinone, ialibinones, and takaneones via ring-closing metathesis reaction

Srikrishna, A. ; Beeraiaha, B. ; Gowri, V. (2009) Enantiospecific approach to the tricyclic core structure of tricycloillicinone, ialibinones, and takaneones via ring-closing metathesis reaction Tetrahedron, 65 (13). pp. 2649-2654. ISSN 0040-4020

Full text not available from this repository.

Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tet.2009.01.096

Abstract

Enantiospecific synthesis of the tricyclic core structure present in the biologically active natural products tricycloillicinone, ialibinones, and takaneones, starting from the readily available campholenaldehyde employing a transannular RCM reaction as the key step, has been accomplished.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Tricyclo[5.3.1.01,5]undecane; (S)-Campholenaldehyde; Enantiospecific Synthesis; RCM Reaction; Diquinanes; Illicinones
ID Code:48788
Deposited On:15 Jul 2011 11:52
Last Modified:15 Jul 2011 11:52

Repository Staff Only: item control page