Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/27597
Title: Isolute®Si-carbonate catalyzes the nitronate addition to both aldehydes and electron-poor alkenes under solvent-free conditions
Authors: Ballini, Roberto
Bosica, Giovanna
Palmieri, Alessandro
Pizzo, Ferdinando
Vaccaro, Luigi
Keywords: Chemical reactions
Nitroalkanes
Aldehydes
Chemistry, Organic
Carbonyl compounds
Issue Date: 2008
Publisher: The Royal Society of Chemistry
Citation: Ballini, R., Bosica, G., Palmieri, A., Pizzo, F., & Vaccaro, L. (2008). Isolute® si-carbonate catalyzes the nitronate addition to both aldehydes and electron-poor alkenes under solvent-free conditions. Green Chemistry, 10(5), 541-544.
Abstract: It has been found that commercial ISOLUTE® Si-carbonate catalyzes both nitroaldol and Michael reactions, from nitroalkanes and under solvent-free conditions, allowing satisfactory to good yields of nitroalkanols and γ-nitro-functionalized carbonyl and cyano derivatives. In addition, a one-pot Henry-Michael reaction can be performed.
URI: https://www.um.edu.mt/library/oar//handle/123456789/27597
Appears in Collections:Scholarly Works - FacSciChe

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