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萘醌芳基化催化反应研究进展
引用本文:张春伶,包永胜,照日格图. 萘醌芳基化催化反应研究进展[J]. 工业催化, 2015, 23(2): 92-97. DOI: 0.3969/j.issn.1008-1143.2015.02.002
作者姓名:张春伶  包永胜  照日格图
作者单位:内蒙古师范大学化学与环境科学学院 内蒙古自治区绿色催化重点实验室,内蒙古 呼和浩特 010022
基金项目:国家重点基础研究发展计划(973计划)前期研究专项(2014CB460609);内蒙古自治区重大基础研究开放课题(20130902)
摘    要:萘醌类化合物由于具有多样生物活性,广泛应用于医药、农药和染料等多相领域,关于萘醌类化合物的合成有很大的研究价值。综述近年来萘醌与各种芳香族化合物的C—C偶联反应的研究报道,包括萘醌与苯硼酸、芳烃、苯基金属卤化物、苯肼和苯胺的芳基化反应等,探讨这些催化反应的反应机理,并比较各种方法的优缺点。现有的合成芳基萘醌的方法存在选择性和收率较低、催化剂不能回收利用和反应液难以分离等缺陷。探索更加绿色环保、催化剂廉价易得且能重复使用的多相催化体系对萘醌芳基化反应的发展具有显著意义。

关 键 词:精细化学工程  萘醌  C-C偶联  芳基化  

Research progress in catalytic reaction for arylation of naphthoquinone
Zhang Chunling , Bao Yongsheng , Bao Zhaorigetu. Research progress in catalytic reaction for arylation of naphthoquinone[J]. Industrial Catalysis, 2015, 23(2): 92-97. DOI: 0.3969/j.issn.1008-1143.2015.02.002
Authors:Zhang Chunling    Bao Yongsheng    Bao Zhaorigetu
Affiliation:Inner Mongolia Key Laboratory of Green Catalysis, College of Chemistry and Environmental Science, Inner Mongolia Normal University, Hohhot 010022, Inner Mongolia, China
Abstract:Naphthoquinones have been widely applied in medicine,pesticide,dye and other fields due to their various biological activites,so the synthesis of naphthoquinones is of great significance.The study of C-C coupling reaction of naphthoquinones with aromatic compounds in recent years was reviewed,and the reaction mechanisms as well as the advantages and disadvantages of the synthetic methods were discussed in this paper.The arylation reactions,including naphthoquinone with benzeneboronic acid,arene,phenyl metal halide,phenylhydrazine and phenylamine were introduced.The present synthetic methods had the disadvantages of low selectivity,low yield,difficult recycle of catalysts and difficult separation of reaction solution.Therefore,it has notable significance to investigate the green heterogeneous catalytic systems and the catalysts which is cheap, easy to separate and can be repeated use in the development of naphthoquinone arylation.
Keywords:fine chemical engineering  naphthoquinone  C-C coupling  arylation
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