PALLADIUM-CATALYZED CONSECUTIVE ONE-POT REACTION OF ACETYLENES WITH ALLYL BROMIDE AND ORGANOTIN COMPOUNDS

被引：23

作者：

KOSUGI, M ^{[1
]}

SAKAYA, T ^{[1
]}

OGAWA, S ^{[1
]}

MIGITA, T ^{[1
]}

机构：

[1] TOKAI UNIV, SCH HIGH TECHNOL HUMAN WELFARE, SHIZUOKA 41003, JAPAN

来源：

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN | 1993年 / 66卷 / 10期

关键词：

D O I：

10.1246/bcsj.66.3058

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Allyl bromide adds to a terminal acetylene under the palladium complex to give 1-bromo-1,4-pentadiene which can further react with organotin compounds without further addition of palladium complex to give 1-substituted 1,4-pentadiene. These two reactions involving different catalytic species can be composed into the consecutive one-pot process.

引用

页码：3058 / 3061

页数：4

共 13 条

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