有機合成化学協会誌
Online ISSN : 1883-6526
Print ISSN : 0037-9980
ISSN-L : 0037-9980
位置選択的リチオ化反応を利用したインドール環の効率的官能化
岩尾 正倫福田 勉
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ジャーナル フリー

2002 年 60 巻 7 号 p. 691-700

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This article reviews the regioselective lithiations of indole derivatives. The C-2 lithiation can be readily achieved by utilizing directed lithiation promoted by a protecting (directing) group on indole nitrogen. The C-3 lithiation has been carried out mainly by halogen-lithium exchange of N-protected 3-bromo (or iodo) indoles. The lithiation at the benzenoid portion of indole has been performed by several unique methods, which are designed by considering the specific properties of indole ring and N-protecting groups. These regioselective lithiations have been nicely applied for the short-step synthesis of a number of indole-containing natural products.

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