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


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2016-02

AUTHORS

A. F. Asachenko, V. N. Valaeva, V. A. Kudakina, D. V. Uborsky, V. V. Izmer, D. S. Kononovich, A. Z. Voskoboynikov

ABSTRACT

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.

PAGES

456-463

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-016-1321-3

DOI

http://dx.doi.org/10.1007/s11172-016-1321-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1008510801


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