Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/99295
Title: The nitroaldol (Henry) reaction as the key step for the synthesis of some natural products
Other Titles: Frontiers in Natural Product Chemistry Vol 1
Authors: Ballini, Roberto
Bosica, Giovanna
Fiorini, Dennis
Palmieri, Alessandro
Keywords: Natural products -- Synthesis
Heterogeneous catalysis
Nitroalkanes -- Synthesis
Nitro compounds -- Synthesis
Issue Date: 2005
Publisher: Bentham Science Publishers
Citation: Ballini, R., Bosica, G., Fiorini, D., & Palmieri, A. (2005). The nitroaldol (Henry) reaction as the key step for the synthesis of some natural products. In Atta-ur-Rahman, M. Iqbal Choudhary, & Khalid M. Khan (Eds.), Frontiers in Natural Product Chemistry, 1 (pp. 37-41). Bentham Science Publishers.
Abstract: The nitroaldol (Henry) reaction although has been discovered more than one century ago is still largely employed as the key step for the synthesis of many targets. The reaction is performed under basic condition by mixing primary or secondary nitroalkanes (and nitromethane) with a carbonyl, allowing the formation of a b-nitroalkanol. The latter shows an high versatility since it can be converted into a lot of different functionalities and many natural products have been prepared using the Henry reaction as the key step. Some of these synthesis will be reported.
URI: https://www.um.edu.mt/library/oar/handle/123456789/99295
ISBN: 9077527044
Appears in Collections:Scholarly Works - FacSciChe

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