Transition metal-mediated oxidations utilizing monomeric iodosyl- and iodylarene species

Результат исследований: Материалы для журналаСтатья

65 Цитирования (Scopus)

Выдержка

Several transition metal-mediated oxidations using hypervalent iodine species are reported. A convenient procedure for preparation of iodylarenes via RuCl3-catalyzed oxidation of iodoarenes has been developed. This procedure allows the generation of highly reactive monomeric iodine(V) species, which are excellent oxidants toward alcohols and hydrocarbons in situ. A broad range of substrates can be oxidized to carbonyl compounds by a tandem catalytic system based on the Ru(III)-catalyzed reoxidation of ArIO to ArIO2 using Oxone® as oxidant. It was shown that electrophilic iodine(III) species, originating from oligomeric iodosylbenzene sulfate (PhIO)3SO3, are efficient oxygenating agents in catalytic oxidation of aromatic hydrocarbons in the presence of metalloporphyrin complexes.

Язык оригиналаАнглийский
Страницы (с-по)5745-5752
Число страниц8
ЖурналTetrahedron
Том66
Номер выпуска31
DOI
СостояниеОпубликовано - 31 июл 2010

Отпечаток

Iodine
Transition metals
Metals
Oxidants
Oxidation
Metalloporphyrins
Aromatic Hydrocarbons
Carbonyl compounds
Catalytic oxidation
Hydrocarbons
Sulfates
Alcohols
Substrates
iodosobenzene
potassium peroxymonosulfuric acid

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Цитировать

Transition metal-mediated oxidations utilizing monomeric iodosyl- and iodylarene species. / Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor Vladimirovich.

В: Tetrahedron, Том 66, № 31, 31.07.2010, стр. 5745-5752.

Результат исследований: Материалы для журналаСтатья

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AU - Nemykin, Victor N.

AU - Zhdankin, Viktor Vladimirovich

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KW - Hypervalent iodine

KW - Oxidation

KW - Porphyrins

KW - Ruthenium

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