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Synthesis of Sulfilimines via Selective S-C Bond Formation in Water.
Chen, Yue; Fang, Dong-Mei; Huang, He-Sen; Nie, Xiao-Kang; Zhang, Shi-Qi; Cui, Xin; Tang, Zhuo; Li, Guang-Xun.
  • Chen Y; Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu, Sichuan 610041, China.
  • Fang DM; University of Chinese Academy of Sciences, Beijing 10049, P.R. China.
  • Huang HS; Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu, Sichuan 610041, China.
  • Nie XK; Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu, Sichuan 610041, China.
  • Zhang SQ; Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu, Sichuan 610041, China.
  • Cui X; Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu, Sichuan 610041, China.
  • Tang Z; Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu, Sichuan 610041, China.
  • Li GX; Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu, Sichuan 610041, China.
Org Lett ; 25(12): 2134-2138, 2023 Mar 31.
Article en En | MEDLINE | ID: mdl-36939573
Sulfilimines are valuable compounds both in organic synthesis and in pharmaceuticals. Here we developed a mild and simplified method for preparation of sulfilimines via selective S-C bond formation rather than traditional S-N bond formation. The method is both attractive and useful for the following reasons: it uses a readily available alkylation reagent such alkyl bromide or alkyl iodide, it uses water as solvent, it is easy to perform, and it is convenient for late-stage diversification of drugs.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article