Cargando…
Chemoselective α-Sulfidation of Amides Using Sulfoxide Reagents
[Image: see text] The direct α-sulfidation of tertiary amides using sulfoxide reagents under electrophilic amide activation conditions is described. Employing convenient and readily available reagents, selective functionalization takes place to generate isolable sulfonium ions en route to α-sulfide...
Autores principales: | Leypold, Mario, D’Angelo, Kyan A., Movassaghi, Mohammad |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680396/ https://www.ncbi.nlm.nih.gov/pubmed/33048547 http://dx.doi.org/10.1021/acs.orglett.0c03160 |
Ejemplares similares
-
Chemoselective α,β‐Dehydrogenation of Saturated Amides
por: Teskey, Christopher J., et al.
Publicado: (2018) -
Imido-substituted triazines as dehydrative condensing reagents for the chemoselective formation of amides in the presence of free hydroxy groups
por: Kitamura, Masanori, et al.
Publicado: (2018) -
Unified
Approach to the Chemoselective α-Functionalization
of Amides with Heteroatom Nucleophiles
por: Gonçalves, Carlos R., et al.
Publicado: (2019) -
A Sulfoxide Reagent for One‐Pot, Three‐Component Syntheses of Sulfoxides and Sulfinamides
por: Saito, Fumito
Publicado: (2022) -
Fe(3)O(4)@BNPs@SiO(2)–SO(3)H as a highly chemoselective heterogeneous magnetic nanocatalyst for the oxidation of sulfides to sulfoxides or sulfones
por: Ghanbari Kermanshahi, Mohammad, et al.
Publicado: (2019)