Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5264963 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
The direct high-yield synthesis without solvent and catalyst, under mild conditions, of eleven novel mono substituted ferrocenylmethyl ethers and amine derivatives from ferrocenemethanol and vicinal oxygenated alcohols and amines is here reported. The peculiar ability of these classes of non acidic compounds to favor the dehydrative nucleophilic substitution is attributed to the presence of vicinal oxygen atoms to the reactive group able to build a hydrogen bonding network with the reactant. The role of carbon dioxide and hexafluoroisopropanol was investigated to support the hypothesis that a template catalysis effect is occurring. The in vitro anti-fungal activity of some of these derivatives was tested on two plant fungi, Botrytis cinerea and Penicillium species, with moderate activity.
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Authors
Suresh Udhavrao Shisodia, Sergio Auricchio, Attilio Citterio, Marco Grassi, Roberto Sebastiano,