Enantioselective Synthesis of the Molluscicidal Furanosesquiterpene Lactones Ricciocarpin A and Ricciocarpin B via Ring Closing Metathesis
Author:
Affiliation:
1. Institut für Organische Chemie, Technische Universität Dresden, Bergstr. 66, 01069 Dresden, Germany
2. Organisch‐Chemisches Institut, Universität Münster, Corrensstr. 40, 48149 Münster, Germany
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/1615-4169%28200208%29344%3A6/7%3C720%3A%3AAID-ADSC720%3E3.0.CO%3B2-%23
Reference45 articles.
1. Sesquiterpenoids from the liverwort Ricciocarpos natans
2. Molluscicidal Properties of Constituents from the LiverwortRicciocarpos natansand of Synthetic Lunularic Acid Derivatives
3. Moose, eine Quelle biologisch aktiver Naturstoffe?
4. Bryophytes, a Source of Biologically Active, Naturally Occurring Material?
5. Synthese von Bryophyten-Inhaltsstoffen 4. Synthesen des Ricciocarpins A
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