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• W2803228873 abstract "We report an efficient protocol for the synthesis of 2,3,5‐trisubstituted furans through the reaction of readily available γ‐acetylenic β‐keto esters with aryl and heteroaryl bromides. The reaction, which involves a 5‐ exo ‐ dig cyclization, coupling, and isomerization of a double bond, proceeds smoothly with very low catalyst loading (0.1 mol‐%), and shows excellent functional‐group tolerance." @default.
• W2803228873 created "2018-06-01" @default.
• W2803228873 creator A5014806050 @default.
• W2803228873 creator A5020337797 @default.
• W2803228873 date "2018-05-25" @default.
• W2803228873 modified "2023-10-16" @default.
• W2803228873 title "Efficient and Functional-Group-Tolerant Synthesis of Substituted Furans through the Pd-Catalyzed 5-<i>exo</i> -<i>dig</i> Cyclization/Coupling of γ-Acetylenic β-Keto Esters with (Hetero)Aryl Bromides" @default.
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• W2803228873 doi "https://doi.org/10.1002/ejoc.201800046" @default.
• W2803228873 hasPublicationYear "2018" @default.
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