李新民,冯芳芳,胡庆红,吴庆,袁泽利.化学通报,2018,81(9):840-846.
低温Suzuki反应合成联苯及三联苯化合物
The Preparation of Biaryls and Terphenyls by the Suzuki Reaction at Low Temperature
投稿时间:2018-05-08  修订日期:2018-06-01
DOI:
中文关键词:  Suzuki 反应  无配体 低温反应  联苯化合物 三联苯
英文关键词:Suzuki  reaction, Ligand-free, Low temperature, Biaryl compounds, Terphenyls
基金项目:国家自然科学基金项目(81660575, 81360471)、贵州省科技厅基础研究项目 [2018]1187.
作者单位E-mail
李新民* 遵义医学院 药学院 lixinmin19@126.com 
冯芳芳 遵义医学院 药学院  
胡庆红 遵义医学院 药学院  
吴庆 遵义医学院 药学院  
袁泽利 遵义医学院 药学院  
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中文摘要:
      发展了一个低温下无配体钯催化溴代芳烃与芳基硼酸的Suzuki反应体系。该体系以醋酸钯为催化剂,无水碳酸钾为碱,乙醇水溶液为溶剂,无需加入任何配体,在0 oC下即可高效催化溴代芳烃与芳基硼酸的Suzuki反应,底物容忍性好,产品分离收率最高达97%;以溴代芳基N-甲基亚氨基二乙酸硼酸酯为砌块分子,通过调控反应温度,实现了砌块分子选择性Suzuki反应,从而一锅合成了不对称三联苯化合物,产品收率最高为81%。
英文摘要:
      The development of a palladium-catalyzed ligand-free Suzuki reaction system of aryl bromides and arylboronic acids at low temperature. Using Pd(OAc)2 as catalyst, K2CO3 as base and aqueous ethanol as solvent, various aryl bromides could couple with arylboronic acids efficiently with the highest product yield up to 97%. Using bromo-phenyl N-methyliminodiacetic acid boronate as building block, the chemoselective Suzuki reactions were proceeded smoothly by controlling reaction temperature, and a series of terphenyls were prepared by one-pot double Suzuki reaction which provided the highest terphenyl yield up to 81%
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