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Synthetic studies toward neovibsanins A and B: construction of the neovibsanin core utilizing palladium(0)-catalyzed carbonylative cyclization with carbon monoxide
Authors:Tomoyuki Esumi  Ming Zhao
Affiliation:Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro-cho, Tokushima 770-8514, Japan
Abstract:The core A-ring of neovibsanins A (1) and B (2), which are potent neurotrophic agents isolated from the leaves of Viburnum awabuki, have been effectively constructed by the intramolecular palladium(0)-catalyzed carbonylative cyclization of alkenyl iodide with carbon monoxide.
Keywords:Neovibsanins A and B   Pd-catalyzed carbonylative cyclization   Neurotrophic activity
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