ArticleChemical science2015
Gold-catalyzed tandem reactions of amide-aldehyde-alkyne coupling and cyclization-synthesis of 2,4,5-trisubstituted oxazoles.
Article in Chemical science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Defluorinative Cyclization of Enamides with Fluoroalkyl Halides Through Two Vicinal C(spAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Bimetallic tandem catalysis-enabled enantioselective cycloisomerization/carbonyl-ene reaction for construction of 5-oxazoylmethyl α-silyl alcohol.Chemical science · 2023Article
- Gold-catalyzed synthesis of oxazoles from alkynyl triazenes and dioxazoles.RSC advances · 2022Article
- Gold Catalyzed Multicomponent Reactions beyond A³ Coupling.Molecules (Basel, Switzerland) · 2018Review
- Alkynyl Thioethers in Gold-Catalyzed Annulations To Form Oxazoles.Angewandte Chemie (International ed. in English) · 2017Article
- Development of a method for the synthesis of 2,4,5-trisubstituted oxazoles composed of carboxylic acid, amino acid, and boronic acid.Beilstein journal of organic chemistry · 2017Article
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We report the first cationic gold(i)-catalyzed one-pot reaction of amide, alkyne and aldehyde followed by cyclization, to successfully access highly substituted oxazoles derivatives in good yields. A single catalyst allows the occurring of this multi-step reaction atom- and step-economically, with water as the only theoretical side product.
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Registered trials
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