Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24682
Title: α-Nitrocycloalkanones as a source of α,ω-dicarboxylic acid dimethyl esters
Authors: Ballini, Roberto
Bosica, Giovanna
Keywords: Chemical reactions
Organic compounds -- Synthesis
Dicarboxylic acids
Issue Date: 1997
Publisher: Pergamon Press
Citation: Ballini, R., & Bosica, G. (1997). α-Nitrocycloalkanones as a source of α,ω-dicarboxylic acid dimethyl esters. Tetrahedron, 53(47), 16131-16138.
Abstract: α,ω-Dicarboxylic acid dimethyl esters are casily obtained by ring cleavage of α-nitrocycloalkanones. Thus, reaction of the latter compounds with three equivalents of potassium persulfate, in methanol and in presence of sulfuric acid at 80°C, provides α,ω-dicarboxylic acid dimethyl esters in high yields. Long-chain, and alkylated α,ω-dicarboxylic acid dimethyl esters can be also efficiently obtained.
URI: https://www.um.edu.mt/library/oar//handle/123456789/24682
Appears in Collections:Scholarly Works - FacSciChe

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