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Iodine-mediated decarboxylative coupling to synthesize ß-sulfonyl-ene-amines/2,3-diarythio-pyrroles from α-amino acids and sodium sulfinates.
Yang, Xiaodong; Yang, Feng; Zhang, Xiaoya.
Afiliação
  • Yang X; Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang 438000, P. R. China. yangxd2014@lzu.edu.cn.
  • Yang F; Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang 438000, P. R. China. yangxd2014@lzu.edu.cn.
  • Zhang X; Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang 438000, P. R. China. yangxd2014@lzu.edu.cn.
Org Biomol Chem ; 22(36): 7321-7326, 2024 Sep 18.
Article em En | MEDLINE | ID: mdl-39171619
ABSTRACT
A novel process has been developed for the selective synthesis of ß-sulfonyl-enamines and 2,3-diarylthiopyrroles. This process utilizes the decarboxylative coupling and ß-C(sp3)-H functionalization of α-amino acids. In this reaction, iodine functions dually as a tandem catalyst to initiate the decarboxylation of α-amino acids and as an oxidant to facilitate the formation of organic sulfides. This innovative approach not only simplifies the synthesis but also enhances the yield and selectivity of the desired products.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Ano de publicação: 2024 Tipo de documento: Article