Cyclopentene-regioselective palladium-catalyzed cycloisomerization under neutral and bis-cationic reaction conditions

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Abstract

A series of 1,6-dienes is cyclized to cyclopentene derivatives under neutral conditions with palladium chloride in ethanol or with in situ generated LPd2+ in acetonitrile. © 2003 Elsevier Science Ltd. All rights reserved.

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Heumann, A., Giordano, L., & Tenaglia, A. (2003). Cyclopentene-regioselective palladium-catalyzed cycloisomerization under neutral and bis-cationic reaction conditions. Tetrahedron Letters, 44(7), 1515–1518. https://doi.org/10.1016/S0040-4039(02)02668-0

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