Some Features of Reaction of 2-Methyl-1,4-naphthoquinone with H-Phosphonium Salts Based on Diphenylphosphine
Nadezhda R. Khasiyatullina, Daut R. Islamov, Vladimir Fedorovich Mironov
Abstract
Nadezhda R. Khasiyatullina, Daut R. Islamov, Vladimir Fedorovich Mironov
Abstract
It was shown that the direction of the reaction of 2-methyl-1,4-naphthoquinone with H-phosphonium salts obtained from diphenylphosphine and trifluoromethanesulfonic or trifluoroacetic acids depends on the nature of the anion. Structure of the obtained mono- and diphosphinates, as well as the quasi-phosphonium salt, was established by NMR spectroscopy and single crystal X-ray diffraction methods.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
It was shown that the direction of the reaction of 2-methyl-1,4-naphthoquinone with H-phosphonium salts obtained from diphenylphosphine and trifluoromethanesulfonic or trifluoroacetic acids depends on the nature of the anion. Structure of the obtained mono- and diphosphinates, as well as the quasi-phosphonium salt, was established by NMR spectroscopy and single crystal X-ray diffraction methods.
Key concepts: Phosphonium, Chemistry, Diphenylphosphine, Phosphonium salt, Salt (chemistry), Medicinal chemistry, Nuclear magnetic resonance spectroscopy, Organic chemistry