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Wiley, Angewandte Chemie International Edition, 43(48), p. 8042-8046, 2009

DOI: 10.1002/anie.200903743

Wiley, Angewandte Chemie, 43(121), p. 8186-8190, 2009

DOI: 10.1002/ange.200903743

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Total Synthesis of Pentabromo- and Pentachloropseudilin, and Synthetic Analogues-Allosteric Inhibitors of Myosin ATPase

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This paper is available in a repository.

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Abstract

Stopping myo: The total syntheses of the title compounds have been achieved using a highly efficient silver(I)- catalyzed cyclization of N-tosyl-homopropargylamines. The pseudilin derivatives represent a novel class of myosin inhibitors. A new allosteric binding pocket of the Dictyostelium myosin-2 motor domain has been identified for pentabromopseudilin (1) by using an X-ray crystal structure determination of the inhibitor-protein complex.