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Australian Journal of Forensic Sciences Volume 48, 2016 - Issue 6
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Influence of base on nitro-aldol (Henry) reaction products for alternative clandestine pathways

Luke M. AndrighettoCentre for Chemistry and Biotechnology, School of Life and Environmental Sciences, Deakin University, Geelong, Australia
,
Luke C. HendersonInstitute for Frontier Materials, Deakin University, Geelong, Australia
,
James R. PearsonVictoria Police Forensic Services Department, Macleod, Australia
,
Paul G. StevensonCentre for Chemistry and Biotechnology, School of Life and Environmental Sciences, Deakin University, Geelong, Australia
&
Xavier A. ConlanCentre for Chemistry and Biotechnology, School of Life and Environmental Sciences, Deakin University, Geelong, AustraliaCorrespondence[email protected]
Pages 684-693 | Received 12 Aug 2015, Accepted 19 Oct 2015, Published online: 22 Jan 2016

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Niloufar Parandeh-Khoozani & Mohsen Moradian. (2021) Synthesis of nitroaldols through the Henry reaction using a copper(II)–Schiff base complex anchored on magnetite nanoparticles as a heterogeneous nanocatalyst. Journal of Coordination Chemistry 74:12, pages 2035-2054.
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Articles from other publishers (1)

Brendan M. Miller, Peter N. Culshaw, Sarah L. Cresswell, Wendy A. Loughlin & Wendy Loa-Kum-Cheung. (2023) Impurity profiling of an alternative pathway to ephedrine/pseudoephedrine and methamphetamine from the precursors benzaldehyde and nitroethane. Forensic Chemistry 36, pages 100540.
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