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Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles.
Matsuzaki, Kohei; Okuyama, Kenta; Tokunaga, Etsuko; Saito, Norimichi; Shiro, Motoo; Shibata, Norio.
Afiliação
  • Matsuzaki K; †Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan.
  • Okuyama K; †Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan.
  • Tokunaga E; †Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan.
  • Saito N; ‡Pharmaceutical Division, Ube Industries, Ltd., Seavans North Building 1-2-1 Shibaura, Minato-ku, Tokyo 105-8449, Japan.
  • Shiro M; §Rigaku Corporation, 3-9-12 Mastubara-cho, Akishima, Tokyo 196-8666, Japan.
  • Shibata N; †Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan.
Org Lett ; 17(12): 3038-41, 2015 Jun 19.
Article em En | MEDLINE | ID: mdl-26023887
ABSTRACT
Novel reagents for the electrophilic introduction of pentafluorosulfanyl (SF5) arenes into target molecules are disclosed. Unsymmetrical diaryliodonium salts 1 having SF5-arenes were synthesized by a one-pot process from iodo-SF5-benzenes 2 in good yields. The SF5-aryliodonium salts 1 were found to be efficient for the electrophilic SF5-arylation of carbon and heterocentered nucleophiles to furnish the corresponding substituted SF5-arenes in good to high yields.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oniocompostos / Sais / Hidrocarbonetos Fluorados / Indicadores e Reagentes / Iodo Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oniocompostos / Sais / Hidrocarbonetos Fluorados / Indicadores e Reagentes / Iodo Idioma: En Ano de publicação: 2015 Tipo de documento: Article