Development of Imino-λ3-iodanes with Improved Reactivity for Metal-Free [2+2+1] Cycloaddition-Type Reactions

Takafumi Baba, Shunsuke Takahashi, Yui Kambara, Akira Yoshimura, Victor N. Nemykin, Viktor V. Zhdankin, Akio Saito

Результат исследований: Материалы для журналаСтатья

5 Цитирования (Scopus)

Выдержка

Aiming at the enhancement of electrophilicity of imino-λ3-iodanes, we have developed (tosylimino)pentafluorophenyl-λ3-iodane, which shows superior reactivity compared to the commonly used (tosylimino)phenyl-λ3-iodane in the [2+2+1]-type synthesis of imidazoles. (Figure presented.).

Язык оригиналаАнглийский
Страницы (с-по)3860-3864
Число страниц5
ЖурналAdvanced Synthesis and Catalysis
Том359
Номер выпуска21
DOI
СостояниеОпубликовано - 10 ноя 2017

Отпечаток

Imidazoles
Cycloaddition
Metals

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

Цитировать

Development of Imino-λ3-iodanes with Improved Reactivity for Metal-Free [2+2+1] Cycloaddition-Type Reactions. / Baba, Takafumi; Takahashi, Shunsuke; Kambara, Yui; Yoshimura, Akira; Nemykin, Victor N.; Zhdankin, Viktor V.; Saito, Akio.

В: Advanced Synthesis and Catalysis, Том 359, № 21, 10.11.2017, стр. 3860-3864.

Результат исследований: Материалы для журналаСтатья

Baba, Takafumi ; Takahashi, Shunsuke ; Kambara, Yui ; Yoshimura, Akira ; Nemykin, Victor N. ; Zhdankin, Viktor V. ; Saito, Akio. / Development of Imino-λ3-iodanes with Improved Reactivity for Metal-Free [2+2+1] Cycloaddition-Type Reactions. В: Advanced Synthesis and Catalysis. 2017 ; Том 359, № 21. стр. 3860-3864.
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abstract = "Aiming at the enhancement of electrophilicity of imino-λ3-iodanes, we have developed (tosylimino)pentafluorophenyl-λ3-iodane, which shows superior reactivity compared to the commonly used (tosylimino)phenyl-λ3-iodane in the [2+2+1]-type synthesis of imidazoles. (Figure presented.).",
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AU - Kambara, Yui

AU - Yoshimura, Akira

AU - Nemykin, Victor N.

AU - Zhdankin, Viktor V.

AU - Saito, Akio

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