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Structure revision of emiline a pyrrolizidine alkaloid from Emilia flammea
Institution:1. Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD 21210, USA;2. Intergrated Image Centre, Johns Hopkins University, Baltimore, MD 21210, USA;3. U.S. Army Research Lab, Aberdeen Proving Ground, MD 21005, USA;1. Department of Chemistry, Mohanlal Sukhadia University, Udaipur 313-001, India;2. Department of Chemistry, University of Rajasthan, Jaipur 302-004, India;3. Faculty of Advanced Life Science, Frontier Research Center for Post-Genome Science and Technology, Hokkaido University, Sapporo 001-0021, Japan;4. Department of Chemistry and Materials Science, Tokyo Institute of Technology, Meguro, Tokyo 152-8551, Japan;1. Max-Planck Institut für Chemische Ökologie, Beutenberg Campus, Hans-Knöll-Strasse 8, 07745, Jena, Germany;2. Jiangsu Key Laboratory for Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences, Qianhu Houcun 1, 210014, Nanjing, China;1. University of Uppsala, Department of Chemsitry—BMC, Box 576, SE-751 23 Uppsala, Sweden;2. National Institute of Chemical Physics and Biophysics, Akadeemia tee 23, 12618 Tallinn, Estonia
Abstract:The structure of emiline, a pyrrolizidine alkaloid isolated fromEmilia flammea has been revised from an 11-membered alkaloid to a 12-membered macrocyclic diester containing otonecine.
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