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

Research output: Contribution to journalArticle

5 Citations (Scopus)

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.).

Original languageEnglish
Pages (from-to)3860-3864
Number of pages5
JournalAdvanced Synthesis and Catalysis
Volume359
Issue number21
DOIs
Publication statusPublished - 10 Nov 2017

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Imidazoles
Cycloaddition
Metals

Keywords

  • Alkynes
  • cycloaddition
  • imidazoles
  • iminoiodanes
  • metal-free

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

Cite this

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.

In: Advanced Synthesis and Catalysis, Vol. 359, No. 21, 10.11.2017, p. 3860-3864.

Research output: Contribution to journalArticle

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. In: Advanced Synthesis and Catalysis. 2017 ; Vol. 359, No. 21. pp. 3860-3864.
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AU - Nemykin, Victor N.

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