Journal of Heterocyclic Chemistry p. 335 - 339 (2002)
Update date:2022-07-30
Topics:
Yamaguchi, Seiji
Hamade, Eriko
Yokoyama, Hajime
Hirai, Yoshiro
Shiotani, Shunsaku
Birch reduction of four furopyridines 1a-d effected the characteristic cleavage of the furan ring, giving ethnylpyridinols 2a-d, vinylpyridinols 3b,d, and ethylpyridinols 4a-d, and the reduction of the furan ring, giving dihydrofuropyridine 5c,d.
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