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Reversible Diels-Alder reactions for the generation of dynamic combinatorial libraries
Authors:Boul Peter J  Reutenauer Philippe  Lehn Jean-Marie
Affiliation:Laboratoire de Chimie Supramoléculaire, ISIS, Université Louis Pasteur, 8, allée Gaspard Monge, BP70028, F67083 Strasbourg, Cedex, France.
Abstract:Condensation reactions between various dienes and dienophiles have been screened for reversibility. Functionalized fulvenes, bearing in particular biological groups, and cyanolefins have been found to react rapidly and reversibly, in the temperature range from -10 to +50 degrees C. These results pave the way for the development of dynamic combinatorial libraries based on reversible Diels-Alder chemistry.
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