期刊
TETRAHEDRON
卷 61, 期 13, 页码 3261-3269出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2004.10.100
关键词
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The lithiation of nine anisylpyridines has been studied. While usual reagents did not react or gave addition products on pyridine ring, the BuLi-LiDMAE (LiDNlAEz=Me2N(CH2)(2)OLi) superbase induced exclusive pyridino directed metallation. The usefulness of this new reaction allowed the efficient preparation of a range of alpha functional pyridylphenols. A successful subsequent cyclisation of an appropriate isomer into corresponding benzofuropyridine was also performed. (c) 2004 Elsevier Ltd. All rights reserved.
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