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Brønsted Acid–Catalyzed Tandem Reaction of 1,4‐Enediones with 2‐Naphthols: Synthesis of 2‐Furylmethylnaphthalenes

Von Wiley-VCH zur Verfügung gestellt

A Brønsted acid-catalyzed tandem reaction of 1,4-enediones with aromatic nucleophiles was developed, affording a series of 2-furylmethylarenes in high yields (up to 98%). The attractive features of this reaction include mild reaction conditions, overall high yields, and water as the only byproduct.


Abstract

A Brønsted acid-catalyzed tandem cyclization/addition reaction of 1,4-enediones with 2-naphthols was developed, affording a series of 2-furylmethylnaphthalenes in high yields (up to 98%). Furthermore, the control experiments revealed the possible reaction pathway and activation mode, which will enrich the research on Brønsted acid catalysis and tandem reactions.

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