N‐Acyl‐Glutarimides: Privileged Scaffolds in Amide N–C Bond Cross‐Coupling Article Swipe
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Guangrong Meng
,
Michal Szostak
·
YOU?
·
· 2018
· Open Access
·
· DOI: https://doi.org/10.1002/ejoc.201800109
· OA: W2809149148
YOU?
·
· 2018
· Open Access
·
· DOI: https://doi.org/10.1002/ejoc.201800109
· OA: W2809149148
In this Microreview, we describe the recent exciting developments in the burgeoning area of amide N–C cross‐coupling enabled by amide bond twist of N ‐acyl‐glutarimides. Since the initial reports in 2015, these amides have been demonstrated to be by far the most reactive amide derivatives in the biologically‐relevant manifold of N–C activation/cross‐coupling, thus stimulating the development of more than 10 previously unknown catalytic modes of reactivity of the amide bond. The capacity of N ‐acyl‐glutarimides as privileged scaffolds to expedite acyl and decarbonylative cross‐couplings by amide N–C cleavage is discussed.
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