Divergent Product Selectivity in Gold- versus Silver-Catalyzed Reaction of 2-Propynyloxy-6-fluoropyridines with Arylamines

Colombe Gronnier 1 Pierre Faudot Dit Bel 1 Guilhem Henrion 1 Søren Krämer 1 Fabien Gagosz 1
1 DCSO - Laboratoire de synthèse organique
Abstract : A study of the reaction of easily accessible 2-propynyloxy-6-fluoropyridines with arylamines under gold or silver catalysis is described. It has been shown that two types of isomeric oxazolopyridine imine derivatives, which represent unusual heterocyclic motifs, can be selectively obtained in moderate to excellent yields depending on the nature of the metal employed.
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Submitted on : Friday, May 23, 2014 - 9:55:38 AM
Last modification on : Thursday, February 7, 2019 - 5:16:34 PM

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Colombe Gronnier, Pierre Faudot Dit Bel, Guilhem Henrion, Søren Krämer, Fabien Gagosz. Divergent Product Selectivity in Gold- versus Silver-Catalyzed Reaction of 2-Propynyloxy-6-fluoropyridines with Arylamines. Organic Letters, American Chemical Society, 2014, 16 (8), pp.2092-2095. ⟨10.1021/ol500939v⟩. ⟨hal-00995310⟩

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