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Inhibition of Homo-coupling of Arylboronic Acids in Ligand Free Pd(ll)-Catalyzed Suzuki Reaction    

Inhibition of Homo-coupling of Arylboronic Acids in Ligand Free Pd(ll)-Catalyzed Suzuki Reaction

文献类型:期刊文献

中文题名:Inhibition of Homo-coupling of Arylboronic Acids in Ligand Free Pd(ll)-Catalyzed Suzuki Reaction

英文题名:Inhibition of Homo-coupling of Arylboronic Acids in Ligand Free Pd(ll)-Catalyzed Suzuki Reaction

作者:陶晓春[1];张月平[1];何天雄[1];沈冬[2]

机构:[1]Laboratory of Organometallic Chemistry, East China University of Science and Technology, Shanghai 200237, China;[2]Laboratory of Chemical Physics, East China University of Science and Technology, Shanghai 200237, China

年份:2007

卷号:25

期号:9

起止页码:1326

中文期刊名:Chinese Journal of Chemistry

外文期刊名:中国化学(英文版)

收录:CSTPCD;;Scopus;CSCD:【CSCD2011_2012】;

语种:中文

中文关键词:homo-coupling;cross-coupling;isopropanol;aryl bromide;arylboronic acid

外文关键词:homo-coupling, cross-coupling, isopropanol, aryl bromide, arylboronic acid

摘要:A series of solvents were examined for the ligand free Pd(II)-catalyzed Suzuki reaction of 4-bromotoluene with phenylboronic acid. It was found that the PdCl2/i-PrOH system could efficiently inhibit the homo-coupling of phenylboronic acid and give a cross-coupling product in high yields. The substrates with a wide variety of functional groups were tolerated in the system. A possible mechanism for this system was proposed.
A series of solvents were examined for the ligand free Pd(II)-catalyzed Suzuki reaction of 4-bromotoluene with phenylboronic acid. It was found that the PdCl2/i-PrOH system could efficiently inhibit the homo-coupling of phenylboronic acid and give a cross-coupling product in high yields. The substrates with a wide variety of functional groups were tolerated in the system. A possible mechanism for this system was proposed.

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