Enantioselective Total Synthesis of the Marine Toxin (−)-Gymnodimine Employing a Barbier-Type Macrocyclization
Author:
Publisher
Wiley
Subject
General Chemistry,Catalysis
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.200903432/fullpdf
Reference66 articles.
1. Gymnodimine, a new marine toxin of unprecedented structure isolated from New Zealand oysters and the dinoflagellate, Gymnodinium sp.
2. The absolute stereochemistry of the New Zealand shellfish toxin gymnodimine
3. New Analogue of Gymnodimine from a Gymnodinium Species
4. Investigations into the cellular actions of the shellfish toxin gymnodimine and analogues
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