Coupling of aromatic aldehydes with aryl halides in the presence of nickel catalysts with diazabutadiene ligands


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Nickel catalysts with diazabutadiene ligands promote cross-coupling of benzaldehydes with aryl halides in the presence of zinc as reducing agent, which leads to the corresponding benzhydrols and benzophenones. The benzophenone percentage considerably increases when lithium chloride additive is used.

作者简介

A. Asachenko

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: voskoboy@med.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

V. Valaeva

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: voskoboy@med.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

V. Kudakina

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: voskoboy@med.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

D. Uborsky

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: voskoboy@med.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

V. Izmer

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: voskoboy@med.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

D. Kononovich

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: voskoboy@med.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

A. Voskoboynikov

Department of Chemistry, M. V. Lomonosov Moscow State University

编辑信件的主要联系方式.
Email: voskoboy@med.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

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