Palladium catalyzed ligand-free Suzuki cross-coupling reactions of benzylic halides with aryl boronic acids under mild conditions
Palladium catalyzed ligand-free Suzuki cross-coupling reactions of benzylic halides with aryl boronic acids under mild conditions
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DOI：
10.1016/j.tetlet.2004.07.073
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发表时间：
2004-09-06
影响因子：
1.8
通讯作者：
Phopase, J
中科院分区：
文献类型：
--
作者：
Bandgar, BP;Bettigeri, SV;Phopase, J
以氯化钯为催化剂，丙酮：水（3：1）为溶剂体系，研究了苄基卤与芳基硼酸的Suzuki偶联反应。该方法具有产物收率高、反应条件温和、无需配体、反应时间短等特点。(C)2004爱思唯尔有限公司保留所有权利。
A highly efficient Suzuki cross-coupling reaction between benzylic halides and aryl boronic acids using palladium chloride as catalyst in acetone:water (3:1) as the solvent system has been developed. High yields of products, mild reaction conditions and short reaction times in the absence of ligand are important features of this method. (C) 2004 Elsevier Ltd. All rights reserved.