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Macrocyclisation of 2-(5-(2-hydroxyethyl)furan-2-yl)acetic acid model compounds of nonactic acid
Authors:Carine Eng  Jean-Mary Simone  Akane Hartenbach  François Loiseau  Reinhard Neier
Institution:(1) Department of Chemistry, University of Neuchatel, Avenue Bellevaux 51, 2007 Neuchatel, Switzerland
Abstract:Abstract  The macrocyclisation of hydroxyethylfuranyl acetic acid and of dehydrogenated model compounds of nonactic acid was investigated to develop a facile synthesis of nonactin analogues. By applying the Yamagushi macrocyclisation to our ω-hydroxyacids, we were able to isolate a mixture of di-, tri-, tetra- and pentameric macrocycles. Graphical abstract   MediaObjects/706_2008_31_Figm_HTML.gif
Keywords:Heterocycles  Macrocycles  Natural product analogues  Nonactin  Protecting groups
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