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Alexander Zhdanko and Prof. Dr. Martin E. Maier Synthesis of gem-Diaurated Species from Alkynols Chemistry - A European Journal 19

Version of Record online: 11 FEB 2013 | DOI: 10.1002/chem.201204491

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Catch the gold fish: A number of enol ether derived diaurated species were synthesized directly from different alkynols and cationic gold complexes in the presence of a non-nucleophilic base (proton sponge; see scheme). The reaction can be easily applied for the in situ generation of diaurated species from all common types of hydroalkoxylation substrates: 5-endo, 5-exo/6-endo, 6-exo/7-endo and even intermolecular types. The reactivity of various gold oxo compounds (LAu)2OH+, (LAu)3O+, and LAuOH (L=phosphine ligand) towards alkynols was also examined.

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