Issue 3, 2005

Regiospecific topochemical reactions controlled by trifluoromethyl directing groups

Abstract

A parallel, offset-stacked orientation was found in the crystal packing of E,E-1,4-di(o-trifluoromethyl)phenyl-1,3-butadiene. UV-irradiation of the powered crystalline sample resulted in a quantitative conversion to a single [2 + 2] cycloaddition product.

Graphical abstract: Regiospecific topochemical reactions controlled by trifluoromethyl directing groups

Supplementary files

Article information

Article type
Communication
Submitted
08 Sep 2004
Accepted
08 Oct 2004
First published
29 Nov 2004

Chem. Commun., 2005, 340-341

Regiospecific topochemical reactions controlled by trifluoromethyl directing groups

J. Liu and K. J. Boarman, Chem. Commun., 2005, 340 DOI: 10.1039/B413898H

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