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• W2092167079 endingPage "8984" @default.
• W2092167079 startingPage "8980" @default.
• W2092167079 abstract "Abstract tert ‐Butoxyacetylene is shown to undergo Sonogashira coupling with aryl iodides to yield aryl‐substituted tert‐butyl ynol ethers. These intermediates participate in a [1,5]‐hydride shift, which results in the extrusion of isobutylene and the generation of aryl ketenes. The ketenes are trapped in situ with multiple nucleophiles or undergo electrocyclic ring closure to yield hydroxynaphthalenes and quinolines." @default.
• W2092167079 created "2016-06-24" @default.
• W2092167079 creator A5086819949 @default.
• W2092167079 creator A5088196532 @default.
• W2092167079 date "2014-06-27" @default.
• W2092167079 modified "2023-10-18" @default.
• W2092167079 title "The Ketene-Surrogate Coupling: Catalytic Conversion of Aryl Iodides into Aryl Ketenes through Ynol Ethers" @default.
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• W2092167079 doi "https://doi.org/10.1002/anie.201405036" @default.
• W2092167079 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4134717" @default.
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• W2092167079 hasPublicationYear "2014" @default.
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