REACTIVITY OF 3,6-DIMETHOXY-3,6-DIMETHYLCYCLOHEXA-1,4-DIENE .2. REGIOSELECTIVE ARYLATION OF ELECTRON-RICH AROMATIC-COMPOUNDS

被引：10

作者：

ALONSO, F

YUS, M

机构：

[1] Departamento de Quimica Orgánica, Facultad de Ciencias, Universidad de Alicante

来源：

TETRAHEDRON | 1991年 / 47卷 / 02期

关键词：

D O I：

10.1016/S0040-4020(01)80926-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of 3,6-dimethoxy-3,6-dimethylcyclohexa-1,4-diene (1) with electron-rich heterocycles (furan, thiophene, pyrrole, 2-methyl-furan, indole) and 1,3,5-trimethoxybenzene in the presence of catalytic amounts of zinc dichloride or concentrated sulfuric acid leads to the corresponding 2-aryl substituted rho-xylenes 4 in good yields and in a regioselective manner.

引用

页码：313 / 316

页数：4