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Enantioselective total synthesis of the phytotoxic lactone herbarumin I

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Fürstner,  Alois
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Radkowski,  Karin
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

Fürstner, A., & Radkowski, K. (2001). Enantioselective total synthesis of the phytotoxic lactone herbarumin I. Chemical Communications, (2), 671-672. doi:10.1039/B101148K.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0024-34C6-8
Abstract
A concise total synthesis of the potent herbicide herbarumin I (1) is presented based on an (E)-selective RCM reaction forging the 10-membered ring of this macrolide.