Cargando…
N-Sulfenylation of β-Lactams: Radical Reaction of N-Bromo-azetidinones by TEMPO Catalysis
[Image: see text] Azetidinones with a sulfenyl group on the β-lactam nitrogen atom show interesting biological activities as antimicrobial agents and enzyme inhibitors. We report in the present study a versatile synthesis of N-sulfenylated azetidinones starting from the corresponding N-bromo derivat...
Autores principales: | Giraldi, Valentina, Giunchino, Francesco, Casacchia, Maria Edith, Cantelli, Andrea, Lucarini, Marco, Giacomini, Daria |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594653/ https://www.ncbi.nlm.nih.gov/pubmed/37769169 http://dx.doi.org/10.1021/acs.joc.3c01759 |
Ejemplares similares
-
Synthesis of N-acyl sulfenamides via copper catalysis and their use as S-sulfenylating reagents of thiols
por: Bai, Ziqian, et al.
Publicado: (2022) -
N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
por: Doraghi, Fatemeh, et al.
Publicado: (2023) -
Synthesis and biological evaluation of Schiff bases and azetidinones of 1-naphthol
por: Kumar, Sushil, et al.
Publicado: (2012) -
Synthesis and Biological Evaluation of New 2-Azetidinones with Sulfonamide Structures
por: Dragostin, Oana Maria, et al.
Publicado: (2013) -
Transition-metal-free synthesis of 3-sulfenylated chromones via KIO(3)-catalyzed radical C(sp(2))–H sulfenylation
por: Guo, Yanhui, et al.
Publicado: (2017)