Conrad–Limpach合成(Conrad–Limpach synthesis)

与β-酮酯在加热条件下发生缩合亚胺,然后进行环化,得到4-羟基喹啉或其衍生物。[1][2][3]


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Conrad-Limpach合成


反应综述:[4][5]

参见

参考资料

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