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The first thiadiazolidine 1-oxide system for phosphine-free palladium-mediated catalysis
journal contributionposted on 28.10.2009 by Benjamin Buckley, Stephen P. Neary
Any type of content formally published in an academic journal, usually following a peer-review process.
We herein report a highly active catalyst system using for the first time a thiadiazolidine 1-oxide as a ligand for palladium in the Mizoroki–Heck reaction. Excellent yields of stilbenes derived from aryl iodides and bromides have been achieved using as little as 0.00002 mol% catalyst. The ligand/palladium system can be stored as a stock solution open to air at room temperature with no observable loss of activity for a period of several weeks/months.