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Direct Synthesis of α-Amino Acid Derivatives by Hydrative Amination of Alkynes.
Feng, Minghao; Tinelli, Roberto; Meyrelles, Ricardo; González, Leticia; Maryasin, Boris; Maulide, Nuno.
Afiliación
  • Feng M; Institute of Organic Chemistry, University of Vienna, Währinger Strasse 38, 1090, Vienna, Austria.
  • Tinelli R; Institute of Organic Chemistry, University of Vienna, Währinger Strasse 38, 1090, Vienna, Austria.
  • Meyrelles R; Vienna Doctoral School in Chemistry, University of Vienna, Währinger Strasse 42, 1090, Vienna, Austria.
  • González L; Institute of Organic Chemistry, University of Vienna, Währinger Strasse 38, 1090, Vienna, Austria.
  • Maryasin B; Institute of Theoretical Chemistry, University of Vienna, Währinger Strasse 17, 1090, Vienna, Austria.
  • Maulide N; Vienna Doctoral School in Chemistry, University of Vienna, Währinger Strasse 42, 1090, Vienna, Austria.
Angew Chem Int Ed Engl ; 62(1): e202212399, 2023 01 02.
Article en En | MEDLINE | ID: mdl-36222199
α-Amino acid derivatives are key components of the molecules of life. The synthesis of α-amino carbonyl/carboxyl compounds is a contemporary challenge in organic synthesis. Herein, we report a practical method for the preparation of α-amino acid derivatives via direct hydrative amination of activated alkynes under mild conditions, relying on sulfinamides as the nitrogen source. Computational studies suggest that the reaction is enabled by a new type of sulfonium [2,3]-sigmatropic rearrangement.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Alquinos / Aminoácidos Idioma: En Revista: Angew Chem Int Ed Engl Año: 2023 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Alquinos / Aminoácidos Idioma: En Revista: Angew Chem Int Ed Engl Año: 2023 Tipo del documento: Article País de afiliación: Austria