A Gold-Catalyzed Acid-Assisted Regioselective Cyclization for the Synthesis of Polysubstituted Oxazoles

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Abstract

Polysubstituted oxazole derivatives are obtained through a regioselective gold-catalyzed reaction of α-alkynylamides and alkynoates in the presence of nitriles. The intermediary obtained gold carbenes are generated by alkyne oxidation with a pyridine N-oxide. Acidic conditions ensure that only one of the two carbonyl oxygen atoms in these intermediates selectively cyclizes to the products in excellent yields.

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Wang, Q., Hoffmann, S., Schießl, J., Rudolph, M., Rominger, F., & Hashmi, A. S. K. (2020). A Gold-Catalyzed Acid-Assisted Regioselective Cyclization for the Synthesis of Polysubstituted Oxazoles. European Journal of Organic Chemistry, 2020(16), 2384–2388. https://doi.org/10.1002/ejoc.201900699

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