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Communication | Regular issue | Vol 20, No. 4, 1983, pp.593-596
Published online, 1st January, 1970
DOI: 10.3987/R-1983-04-0593
One-Pot Synthesis of Furan Systems Bearing 2-Pyridyl Substituent

Otohiko Tsuge, Koyo Matsuda, and Shuji Kanemasa

*Graduate School of Engineering Sciences, Kyushu University, 6-1, Kasuga-koen, Kasuga 816-8580, Japan


The reaction of an anionic intermediate, generated in situ from the lithio derivative of 2-(trimethylsilylmethyl)pyridine and an aromatic nitrile, with α-haloketones such as phenacyl bromide, desyl chloride and 2-bromocyclohexanone provided a route to a one-pot synthesis of rare 2-pyridyl substituted furans. The reaction pathway is also described.