Stannylative Cycloaddition of Enynes Catalyzed by Palladium-iminophosphine
Overview
Authors
Affiliations
Palladium-iminophosphine complex catalyzes stannylative cycloaddition of conjugated enynes using hexabutyldistannoxane as a stannylating agent to afford highly substituted 3-alkenylphenylstannanes regioselectively. Stannylative cross-cycloaddition reactions between different enynes or between enynes and diynes are also achieved. The reaction is successfully applied to a concise synthesis of alcyopterosin N, which has been isolated recently from sub-Antarctic soft coral, Alcyonium paessleri.
Zhang J, Xie Z Chem Sci. 2021; 12(15):5616-5620.
PMID: 34168796 PMC: 8179614. DOI: 10.1039/d0sc07047e.
Secondary Metabolites from Polar Organisms.
Tian Y, Li Y, Zhao F Mar Drugs. 2017; 15(3).
PMID: 28241505 PMC: 5367009. DOI: 10.3390/md15030028.