ARYLATION OF ALKENES BY THE PALLADIUM(II) ACETATE DIALKYL SULFIDE SYSTEM

被引：5

作者：

FUCHITA, Y

TAKEDA, Y

TAGA, M

机构：

[1] Laboratory of Chemistry, College of General Education, Kyushu University, Chuo-ku, Fukuoka, 810, Ropponmatsu

来源：

INORGANICA CHIMICA ACTA | 1994年 / 216卷 / 1-2期

关键词：

CATALYSIS; ARYLATION; PALLADIUM COMPLEXES; ALKENE COMPLEXES;

D O I：

10.1016/0020-1693(93)03736-T

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Reactions of the palladium(II) acetate-dialkyl sulfide system with phenyl substituted ethylenes in aromatic compounds, carried out at 70-degrees-C for 5 h, afford arylated alkenes. Comparing the yields obtained by the system with the previously reported ones, it was found that the system is a more convenient arylating reagent for alkenes.

引用

页码：253 / 256

页数：4

共 15 条

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