SUZUKI-TYPE CROSS-COUPLING REACTIONS USING PALLADIUM-WATER SOLUBLE CATALYST - SYNTHESIS OF FUNCTIONALIZED DIENES

被引：80

作者：

GENET, JP ^{[1
]}

LINQUIST, A ^{[1
]}

BLART, E ^{[1
]}

MOURIES, V ^{[1
]}

SAVIGNAC, M ^{[1
]}

VAULTIER, M ^{[1
]}

机构：

[1] UNIV RENNES 1, CNRS, RECH PHYSICOCHIM STRUCT GRP, F-35042 RENNES, FRANCE

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 09期

关键词：

D O I：

10.1016/0040-4039(95)00026-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The palladium(0) catalyzed cross-coupling of boronic acids or esters conducted with a water soluble catalyst in the presence of organic base allows under mild condition the production of functionalized dienes (60-90% yield).

引用

页码：1443 / 1446

页数：4

共 15 条

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[6] PALLADIUM-CATALYZED REACTIONS IN AQUEOUS-MEDIA - AN EFFICIENT REMOVAL OF ALLYLOXYCARBONYL PROTECTING GROUP FROM OXYGEN AND NITROGEN
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[7] CONVENIENT ONE-POT SYNTHESIS OF VINYLIC SULFIDES FROM THIOALKYNES VIA A CATALYTIC HYDROBORATION COUPLING SEQUENCE
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[10] NEW STEREOSPECIFIC CROSS-COUPLING BY THE PALLADIUM-CATALYZED REACTION OF 1-ALKENYLBORANES WITH 1-ALKENYL OR 1-ALKYNYL HALIDES
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