Mild and regiospecific nuclear iodination of methoxybenzenes and naphthalenes with N-iodosuccinimide in acetonitrile

被引:99
作者
Carreno, MC
Ruano, JLG
Sanz, G
Toledo, MA
Urbano, A
机构
[1] Depto. de Quim. Organ. (C-I), Universidad Autönoma, 28049-Madrid, Cantoblanco
关键词
D O I
10.1016/0040-4039(96)00738-1
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A wide range of methoxy substituted benzenes and naphthalenes were regiospecifically iodinated at para position with N-iodosuccinimide in acetonitrile under mild conditions in excellent yields. Methylanisoles afforded only nuclear iodination products. (C) 1996 Elsevier Science Ltd.
引用
收藏
页码:4081 / 4084
页数:4
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