Abstract:Radical and ionic pathways of fragmentation and the rearrangement of Breslow intermediates coexist, depending on the protonation state of the hydroxyl group.
“…1a). 22 Although several Breslow enolates have already been generated by electrolysis and characterized by UV-vis spectroscopy, [23][24][25][26][27][28] due to their inherent reactivity, the isolation and crystallographic study of these species remains challenging.…”
The highly reactive intermediate (Breslow enolate) of NHC-catalyzed radical reactions has been successfully synthesized and structurally characterized by X-ray diffraction for the first time.
“…1a). 22 Although several Breslow enolates have already been generated by electrolysis and characterized by UV-vis spectroscopy, [23][24][25][26][27][28] due to their inherent reactivity, the isolation and crystallographic study of these species remains challenging.…”
The highly reactive intermediate (Breslow enolate) of NHC-catalyzed radical reactions has been successfully synthesized and structurally characterized by X-ray diffraction for the first time.
Heteroaromatic aldehydes are often used preferentially or exclusively in a range of NHC-catalysed process that proceed through the generation of a reactive diaminoenol or Breslow Intermediate (BI), with the reason...
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