Cyclization of cross-conjugated trienes: the vinylogous Nazarov reaction
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Updated: Jun 23, 2026

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Curtis J Rieder1, Karl J Winberg, F G West
1Department of Chemistry, University of Alberta, E3-43 Gunning-Lemieux Chemistry Centre, Edmonton, AB, T6G 2G2, Canada.
Abstract:
Cross-conjugated trienoates can be readily prepared from 1,4-pentadien-3-one precursors via a 2-step process: 1,2-addition of lithiated ethynyl ethyl ether followed by rearrangement of the resulting propargylic alcohol with catalytic VO(acac)(2). Treatment of the trienoates with stoichometric (TiCl(4)) or catalytic (Sc(OTf)(3)) Lewis acid provided conjugated alkylidenecyclopentenes via an apparent vinylogous Nazarov cyclization.
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