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Modular synthesis of triazoles from 2-azidoacrylamides having a nucleophilic amino group.
Takemura, Hinano; Orimoto, Gaku; Kobayashi, Akihiro; Hosoya, Takamitsu; Yoshida, Suguru.
Afiliação
  • Takemura H; 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.
  • Orimoto G; 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.
  • Kobayashi A; 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; 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.
  • 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.
Org Biomol Chem ; 20(30): 6007-6011, 2022 08 03.
Article em En | MEDLINE | ID: mdl-35201255
ABSTRACT
Assembling methods using 2-azidoacrylamides having a nucleophilic amino group are disclosed. Divergent transformations of the amine-type trivalent platform were accomplished with a wide variety of electrophiles to obtain a broad range of 2-azidoacrylamides involving a fluorosulfonyl group-containing trivalent platform. Consecutive click conjugations including triazole formation, thiol-ene-type 1,4-addition, and SuFEx reactions realized the efficient assembly of easily available simple modules.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triazóis / Química Click Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triazóis / Química Click Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão