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Phosphorus, Sulfur, and Silicon and the Related Elements Volume 192, 2017 - Issue 6: Harry Hudson Special Issue
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Original Articles

Diethyl boronobenzylphosphonates as substrates in Suzuki–Miyaura reaction

Agata RydzewskaDepartment of Bioorganic Chemistry, Faculty of Chemistry, Wrocław University of Science and Technology, Wrocław, Poland
,
Anna MangoldDepartment of Bioorganic Chemistry, Faculty of Chemistry, Wrocław University of Science and Technology, Wrocław, Poland
,
Weronika WanatDepartment of Bioorganic Chemistry, Faculty of Chemistry, Wrocław University of Science and Technology, Wrocław, Poland
&
Paweł KafarskiDepartment of Bioorganic Chemistry, Faculty of Chemistry, Wrocław University of Science and Technology, Wrocław, PolandCorrespondence[email protected]
Pages 758-762 | Received 05 Jan 2017, Accepted 11 Jan 2017, Published online: 25 May 2017
 
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GRAPHICAL ABSTRACT

ABSTRACT

N-substituted boronobenzylphosphonates were evaluated as substrates in Suzuki–Miyaura coupling catalyzed by tetrakis(triphenylphosphine)palladium(0) and complex of palladium acetate and (2-biphenyl)dicyclohexylphosphine. It was proven that they may be considered as useful substrates for the preparation of functionalized aminophosphonates.

Funding

The work was financed by a statutory activity subsidy from the Polish Ministry of Science and Higher Education for the Faculty of Chemistry of Wrocław University of Science and Technology.

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