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Target-driven selection in a dynamic nitrone library
Authors:Turega Simon M  Lorenz Christiane  Sadownik Jan W  Philp Douglas
Institution:EaStCHEM and Centre for Biomolecular Sciences, School of Chemistry, University of St Andrews, St Andrews, Fife, UKKY16 9ST. d.philp@st-andrews.ac.uk.
Abstract:Nitrones undergo dynamic exchange in chloroform at room temperature through two mechanisms-hydrolysis and recombination or hydroxylamine addition/elimination; this dynamic exchange is harnessed to select a nitrone-based bis(amidopyridine) receptor for diacids from a group of four nitrones through its binding to a glutaric acid-based target.
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