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- W3131608088 endingPage "10642" @default.
- W3131608088 startingPage "10637" @default.
- W3131608088 abstract "The development of new methodologies enabling a facile access to valuable heterocyclic frameworks still is an important subject of research. In this context, we describe a dual catalytic cycle merging C-H alkynylation of phenols and oxy-alkynylation of the newly introduced triple bond by using a unique redox property and the carbophilic π acidity of gold. Mechanistic studies support the participation of a bimetallic gold-silver species. The one-pot protocol offers a direct, simple, and regio-specific approach to 3-alkynyl benzofurans from readily available phenols. A broad range of substrates, including heterocycles, is transferred with excellent functional group tolerance. Thus, this methodology can be used for the late-stage incorporation of benzofurans." @default.
- W3131608088 created "2021-03-01" @default.
- W3131608088 creator A5002879988 @default.
- W3131608088 creator A5020325164 @default.
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- W3131608088 creator A5084613894 @default.
- W3131608088 creator A5084670164 @default.
- W3131608088 date "2021-03-30" @default.
- W3131608088 modified "2023-10-16" @default.
- W3131608088 title "Au–Ag Bimetallic Catalysis: 3‐Alkynyl Benzofurans from Phenols via Tandem C−H Alkynylation/Oxy‐Alkynylation" @default.
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