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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2020 Volume 30, Issue 2, Pages 236–237 (Mi mendc1160)

This article is cited in 2 papers

Communications

Synthesis of cinnamyl substituted dihydrofuranones by the Heck cross-coupling reaction

T. V. Ghochikyana, A. S. Vardanyanab, M. A. Samvelyana, A. S. Galstyana, P. Langerb

a Department of Chemistry, Yerevan State University, Yerevan, Armenia
b Institut für Chemie, Universität Rostock, Rostock, Germany

Abstract: The Heck cross-coupling of 3-allyldihydrofuran-2(3H)-ones with aryl bromides [Pd(OAc)3, P(o-Tol)3] afforded the corresponding 3-cinnamyl derivatives. The structure of the products was confirmed by NMR spectroscopy, mass spectrometry and X-ray diffraction.

Keywords: dihydrofuran-2(3H)-ones, cross-coupling, Heck reaction, arylation, aryl bromides, tri(o-tolyl)phosphine, cinnamyl group..

Language: English

DOI: 10.1016/j.mencom.2020.03.036



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