Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24407
Title: The Michael reaction of nitroalkanes with conjugated enones in aqueous media
Authors: Ballini, Roberto
Bosica, Giovanna
Keywords: Nitroalkanes
Carbonyl compounds
Chemical reactions
Catalysts -- Analysis
Issue Date: 1996
Publisher: Pergamon Press
Citation: Ballini, R., & Bosica, G. (1996). The Michael reaction of nitroalkanes with conjugated enones in aqueous media. Tetrahedron Letters, 37(44), 8027-8030.
Abstract: The Michael reaction of various nitroalkanes with conjugated enones can be performed in NaOH 0.025 M and in the presence of cetyltrimethylammonium chloride (CTACl) as cationic surfactant, without any organic solvent. Good yields of the products are obtained even with hindered starting materials.
URI: https://www.um.edu.mt/library/oar//handle/123456789/24407
Appears in Collections:Scholarly Works - FacSciChe

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