Furopyridines. XXXI. Birch reduction of furopyridines
作者:Seiji Yamaguchi、Eriko Hamade、Hajime Yokoyama、Yoshiro Hirai、Shunsaku Shiotani
DOI:10.1002/jhet.5570390215
日期:2002.3
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.
桦木还原四个呋喃吡啶1a-d可实现呋喃环的特征裂解,从而得到乙炔吡啶2a-d,乙烯基吡啶3b,d和乙基吡啶4a-d,并还原呋喃环从而生成二氢呋喃吡啶5c,d。