Issue 29, 2009

Two-directional ring-opening cross-metathesis

Abstract

Two-directional ring-opening cross-metathesis of a range of cyclic alkenes with a variety of electron deficient alkenes has been accomplished; it was found that the process is quite general and gives complete selectivity for the E,E-dienes, making this a very useful and high-yielding protocol for two-directional chain synthesis.

Graphical abstract: Two-directional ring-opening cross-metathesis

Supplementary files

Article information

Article type
Communication
Submitted
31 Mar 2009
Accepted
15 May 2009
First published
10 Jun 2009

Chem. Commun., 2009, 4399-4401

Two-directional ring-opening cross-metathesis

S. J. Roe, J. Legeay, D. Robbins, P. Aggarwal and R. A. Stockman, Chem. Commun., 2009, 4399 DOI: 10.1039/B906301C

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