Enantioselective total synthesis of the phytotoxic lactone herbarumin I
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.
* Corresponding authors
a
Max-Planck-Institut für Kohlenforschung, D-45470, Mülheim/Ruhr, Germany.
E-mail:
fuerstner@mpi-muelheim.mpg.de;
Fax: +49 208 306 2994;
Tel: +49 208 306 2342
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.
Enantioselective total synthesis of the phytotoxic lactone herbarumin I
A. Fürstner and K. Radkowski, Chem. Commun., 2001, 671 DOI: 10.1039/B101148K
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