Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24897
Title: Fast diastereoselective Baylis–Hillman reaction by nitroalkenes : synthesis of di- and triene derivatives
Authors: Ballini, Roberto
Barboni, Luciano
Bosica, Giovanna
Fiorini, Dennis
Mignini, Emanuela
Palmieri, Alessandro
Keywords: Nitroalkanes
Nitro compounds
Allyl compounds
Issue Date: 2004
Publisher: Pergamon Press
Citation: Ballini, R., Barboni, L., Bosica, G., Fiorini, D., Mignini, E., & Palmieri, A. (2004). Fast diastereoselective Baylis–Hillman reaction by nitroalkenes : synthesis of di- and triene derivatives. Tetrahedron, 60(23), 4995-4999.
Abstract: The Baylis–Hillman reaction is performed using nitroalkenes as activated alkenes, ethyl-2-bromomethylacrylate as electrophilic acceptor and DBU as catalyst base. Nitro dienes are obtained in good yields and very short reaction times. Moreover, starting from appropriate nitroalkenes it is possible to realize one pot the synthesis of trienic systems.
URI: https://www.um.edu.mt/library/oar//handle/123456789/24897
Appears in Collections:Scholarly Works - FacSciChe

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