Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/99635
Title: A novel, two-step, mild and simple synthesis of β-, γ and δ-oxo esters from ω-nitro esters
Authors: Ballini, Roberto
Bosica, Giovanna
Keywords: Chemistry, Organic
Organic compounds -- Synthesis
Esters -- Analysis
Nitroalkenes -- Synthesis
Issue Date: 1993
Publisher: Turpin, Letchworth
Citation: Ballini, R., & Bosica, G. (1993). A novel, two-step, mild and simple synthesis of β-, γ and δ-oxo esters from ω-nitro esters. Journal of Chemical Research, Synopses, 435.
Abstract: Since the first example of the Claisen condensation was discovered more than a century ago, β-oxo esters have become one of the most important intermediates in organic synthesis. In addition, y- and δ-oxo esters are highly useful compounds because five- or six-membered carbocycles, and various heterocycles such as lactones, β-lactam antibiotics, isoquinolines and lactonic sex pheromones, are readily accessible from them. Although they have been synthesized by a variety of approaches, several of the existing methods follow lengthy procedures and/or involve expensive chemicals. [excerpt]
URI: https://www.um.edu.mt/library/oar/handle/123456789/99635
ISSN: 03082342
Appears in Collections:Scholarly Works - FacSciChe

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