Total synthesis of the antibiotic elansolid B1
Arne Weber1, Richard Dehn, Nadin Schläger
1Institut für Organische Chemie und Biomolekulares Wirkstoffzentrum (BMWZ), Leibniz Universität Hannover , Schneiderberg 1B, 30167 Hannover, Germany.
Organic Letters
|January 8, 2014
Abstract:
The antibiotic elansolid B1 was prepared by a convergent strategy that relied on a highly diastereoselective, biomimetic intramolecular Diels-Alder cycloaddition (IMDA) that furnished the tetrahydroindane unit. Other key features are a double Sonogashira cross-coupling and a substrate-controlled Yamamoto aldol reaction.
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