Synthetic studies toward neovibsanins A and B: construction of the neovibsanin core utilizing palladium(0)-catalyzed carbonylative cyclization with carbon monoxide |
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Authors: | Tomoyuki Esumi Ming Zhao |
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Affiliation: | Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro-cho, Tokushima 770-8514, Japan |
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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. |
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Keywords: | Neovibsanins A and B Pd-catalyzed carbonylative cyclization Neurotrophic activity |
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