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


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Resumo

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.

Sobre autores

A. Asachenko

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

Email: voskoboy@med.chem.msu.ru
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

V. Valaeva

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

Email: voskoboy@med.chem.msu.ru
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

V. Kudakina

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

Email: voskoboy@med.chem.msu.ru
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

D. Uborsky

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

Email: voskoboy@med.chem.msu.ru
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

V. Izmer

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

Email: voskoboy@med.chem.msu.ru
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

D. Kononovich

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

Email: voskoboy@med.chem.msu.ru
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

A. Voskoboynikov

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

Autor responsável pela correspondência
Email: voskoboy@med.chem.msu.ru
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

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