Issue 18, 1997
From the journal:

Chemical Communications

Supramolecular control of the photochemistry of stilbenes by cyclodextrins

Wolfgang Herrmann,   Susanne Wehrle  and  Gerhard Wenz  

Abstract

Upon UV irradiation in the presence of β-cyclodextrin, (E)-4,4′-bis(dimethylammoniomethyl)stilbene is transformed to the (Z)-isomer, but in the presence of γ-cyclodextrin only the [2 + 2]-cycloaddition products are obtained; the products are a molecular imprint of the cavity of the cyclodextrin.

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Article information

DOI
https://doi.org/10.1039/A703485G
Article type
Paper

Chem. Commun., 1997, 1709-1710

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Supramolecular control of the photochemistry of stilbenes by cyclodextrins

W. Herrmann, S. Wehrle and G. Wenz, Chem. Commun., 1997, 1709 DOI: 10.1039/A703485G

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