Article
A direct synthesis of trichodiene
The Journal of Organic Chemistry
Document Type
Article
Disciplines
Publication Version
Published Version
Publication Date
2-1-1986
DOI
10.1021/jo00354a018
Abstract
The synthesis of trichodiene via the Ireland modification of the Claisen rearrangement is described. The enol ether resulting from the rearrangement functions as a protecting group during two reduction steps. The enol ether diastereomers can be conveniently separated by flash chromatography.
Copyright Owner
American Chemical Society
Copyright Date
1986
Language
en
File Format
application/pdf
Citation Information
George A. Kraus and P.J. Thomas. "A direct synthesis of trichodiene" The Journal of Organic Chemistry Vol. 51 Iss. 4 (1986) p. 503 - 505 Available at: http://works.bepress.com/george_kraus/27/
Reprinted (adapted) with permission from The Journal of Organic Chemistry, 51(4); 503-505. Doi: 10.1021/jo00354a018. Copyright 1986 American Chemical Society.