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Updated: Jul 25, 2026

Preparation and Use of Carbonyl-decorated Carbenes in the Activation of White Phosphorus
Published on: October 3, 2014
Cyclization of carbonyl groups onto alkynes upon reaction with IPy2BF4 and their trapping with nucleophiles: a
José Barluenga1, Henar Vázquez-Villa, Alfredo Ballesteros
1Instituto Universitario de Química Organometálica Enrique Moles-Unidad Asociada al C.S.I.C., Universidad de Oviedo, Julián Claveria 8, 33006 Oviedo, Spain. barluenga@sauron.quimica.uniovi.es
Abstract:
Iodonium ions liberated from bis(pyridine)iodonium(I) tetrafluoroborate react with ortho-alkynyl-substituted carbonyl compounds and different nucleophiles to give valuable iodinated heterocycles at room temperature, through a new and metal-free reaction sequence. Interestingly, the nature of the nucleophile can be widely modified, and not only alcohols but also several carbon-based nucleophiles can be nicely used.
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