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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 35, 2005 - Issue 13
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Original Articles

Preparation of 4‐Arylcyclopentenes by Sequential Diallylation of Arylaldehydes and Ring‐Closing Metathesis

Anne‐Catherine Durand Laboratoire de Synthèse Organique, UMR 6180 CNRS and Université Paul Cézanne (Aix‐Marseille III): Chirotechnologies: Catalyse et biocatalyse, Faculté de St‐Jérôme, Marseille, France
,
Lamia Brahmi Laboratoire de Synthèse Organique, Université d'Oran Es Sénia, Oran, Algeria
,
Mokhtar Lahrech Laboratoire de Synthèse Organique, Université d'Oran Es Sénia, Oran, Algeria
,
Salih Hacini Laboratoire de Synthèse Organique, Université d'Oran Es Sénia, Oran, Algeria
&
Maurice Santelli Laboratoire de Synthèse Organique, UMR 6180 CNRS and Université Paul Cézanne (Aix‐Marseille III): Chirotechnologies: Catalyse et biocatalyse, Faculté de St‐Jérôme, Marseille, FranceCorrespondence[email protected]
Pages 1825-1833 | Received 04 Feb 2005, Published online: 15 Aug 2006
 
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Abstract

Allylsilane diallylation of aryl aldehydes followed by ring closure metathesis leads to 4‐arylcyclopentenes in good yields.

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Related Research Data

A Precision Ethylene-Styrene Copolymer with High Styrene Content from Ring-Opening Metathesis Polymerization of 4-Phenylcyclopentene.
Source: Wiley

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