Campus Units

Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

2-1986

Journal or Book Title

The Journal of Organic Chemistry

Volume

51

Issue

4

First Page

503

Last Page

505

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.

Comments

Reprinted (adapted) with permission from The Journal of Organic Chemistry, 51(4); 503-505. Doi: 10.1021/jo00354a018. Copyright 1986 American Chemical Society.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

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