Issue 1, 2008
From the journal:

Photochemical & Photobiological Sciences

Lignans by photo-oxidation of propenyl phenols

Marina DellaGreca,*a   Maria R. Iesce,*a   Lucio Previtera,a   Raffaella Purcaro,a   Maria Rubinoa  and  Armando Zarrellia  

* Corresponding authors

a Dipartimento di Chimica Organica e Biochimica, Complesso Universitario Monte Sant'Angelo, Via Cinthia 4, I-80126 Naples, Italy
E-mail: dellagre@unina.it, iesce@unina.it
Fax: +39 081 674393
Tel: +39 081 674162

Abstract

Dimeric cyclic or acyclic lignan derivatives have been obtained from isoeugenol under light induced oxidations (mainly by MB-sensitized photooxygenation in water/CH3CN or di-tert-butyl peroxide photo-oxidation). Coniferyl alcohol gives lignans only under peroxide-mediated photo-oxidation while ferulic acid was unreactive under both conditions.

Graphical abstract: Lignans by photo-oxidation of propenyl phenols

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Article information

DOI
https://doi.org/10.1039/B707933H
Article type
Paper
Submitted
24 May 2007
Accepted
15 Oct 2007
First published
26 Oct 2007

Photochem. Photobiol. Sci., 2008,7, 28-32

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Lignans by photo-oxidation of propenyl phenols

M. DellaGreca, M. R. Iesce, L. Previtera, R. Purcaro, M. Rubino and A. Zarrelli, Photochem. Photobiol. Sci., 2008, 7, 28 DOI: 10.1039/B707933H

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