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dc.contributor.authorChen, Hu
dc.contributor.authorHuang, Zhongbin
dc.contributor.authorHu, Xiaoming
dc.contributor.authorTang, Guo
dc.contributor.author唐果
dc.contributor.authorXu, Pengxiang
dc.contributor.authorZhao, Yufen
dc.contributor.author赵玉芬
dc.contributor.authorCheng, Chien-Hong(Natl Tsing Hua Univ, Dept Chem)
dc.date.accessioned2012-03-13T00:51:53Z
dc.date.available2012-03-13T00:51:53Z
dc.date.issued2011-03-09
dc.identifier.citationJ. Org. Chem., 2011, 76 (7): 2338–2344zh_CN
dc.identifier.issn0022-3263
dc.identifier.urihttp://dx.doi.org/doi:10.1021/jo2000034
dc.identifier.uriWOS:000288692000051
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/11723
dc.description.abstractThe Suzuki-Miyaura cross-coupling of aryl phosphates using Ni(PCy(3))(2)Cl(2) as an inexpensive, bench-stable catalyst is described. Broad substrate scope and high efficiency are demonstrated by the syntheses of more than 40 biaryls and by constructing complex organic molecules. The poor reactivity of aryl phosphates relative to aryl halides is successfully employed to construct polyarenes by selective cross-coupling using Pd and Ni catalysts.zh_CN
dc.description.sponsorshipChinese National Natural Science Foundation[20732004, 20972130, 21075103]; Fujian[2009HZ0004-1]zh_CN
dc.language.isoenzh_CN
dc.publisherAMER CHEMICAL SOCzh_CN
dc.titleNickel-Catalyzed Cross-Coupling of Aryl Phosphates with Arylboronic Acidszh_CN
dc.typeArticlezh_CN


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