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Synthesis of benzo[b]furans from alkynyl sulfoxides and phenols by the interrupted Pummerer reaction.
Kobayashi, Akihiro; Matsuzawa, Tsubasa; Hosoya, Takamitsu; Yoshida, Suguru.
Afiliación
  • Kobayashi A; Department of Biological Science and Technology, Faculty of Advanced Engineering, Tokyo University of Science 6-3-1 Niijuku Katsushika-ku Tokyo 125-8585 Japan s-yoshida@rs.tus.ac.jp.
  • Matsuzawa T; Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU) 2-3-10 Kanda-Surugadai Chiyoda-ku Tokyo 101-0062 Japan.
  • Hosoya T; Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU) 2-3-10 Kanda-Surugadai Chiyoda-ku Tokyo 101-0062 Japan.
  • Yoshida S; Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU) 2-3-10 Kanda-Surugadai Chiyoda-ku Tokyo 101-0062 Japan.
RSC Adv ; 13(2): 839-843, 2023 Jan 03.
Article en En | MEDLINE | ID: mdl-36686947
ABSTRACT
The interrupted Pummerer reaction of alkynyl sulfoxides with phenols is disclosed. A wide range of benzo[b]furans were efficiently synthesized through unexplored electrophilic activation of the electron-deficient alkynyl sulfinyl group. Based on the good availability of alkynyl sulfoxides, we successfully prepared various functionalized benzo[b]furans from readily available alkynes, thiosulfonates, and phenols.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2023 Tipo del documento: Article