Cationic palladium(II)-catalyzed addition of arylboronic acids to nitriles. One-step synthesis of benzofurans from phenoxyacetonitriles.

Cationic palladium(II)-catalyzed addition of arylboronic acids to nitriles. One-step synthesis of benzofurans from phenoxyacetonitriles.
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DOI:
10.1021/ol062438v
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发表时间:
2006-11
期刊:
影响因子:
5.2
通讯作者:
Baowei Zhao;Xiyan Lu
Baowei Zhao;Xiyan Lu
中科院分区:
化学1区
文献类型:
--
作者:
Baowei Zhao;Xiyan Lu

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【结构:开发了一种阳离子钯络合物催化的芳基硼酸与腈的加成反应,以中等至良好的产率生成芳基酮。以[(bpy)Pd+(micro-OH)]2(-OTf)2或[(bpy)Pd 2+(H2O)2](-OTf)2为催化剂,由苯氧基乙腈一步合成苯并呋喃。
[Structure: see text] A cationic palladium complex catalyzed addition of arylboronic acids to nitriles to yield aryl ketones with moderate to good yields was developed. A one-step synthesis of benzofurans from phenoxyacetonitriles under the catalysis of [(bpy)Pd+(micro-OH)]2(-OTf)2 or [(bpy)Pd2+(H2O)2](-OTf)2 was developed which showed that the cationic palladium catalyst is highly active for these addition reactions.