Metal-Free Aminocarbonylation of p-Quinone Methides with Isocyanides: Synthesis of Sterically Hindered α-Arylated Acetamides.
Aminocarbonylation
Isocyanide
Sterically Hindered α-Arylated Acetamides
p-Quinone methide
Journal
Chemistry, an Asian journal
ISSN: 1861-471X
Titre abrégé: Chem Asian J
Pays: Germany
ID NLM: 101294643
Informations de publication
Date de publication:
17 Oct 2022
17 Oct 2022
Historique:
revised:
18
08
2022
received:
17
06
2022
pubmed:
21
8
2022
medline:
22
10
2022
entrez:
20
8
2022
Statut:
ppublish
Résumé
The synthesis of sterically hindered α-arylated acetamides generally requires a multistep reaction sequence and is also difficult to access due to steric constraints. This protocol allows the synthesis of sterically hindered α-arylated acetamides in moderate to high yields via 1,6-addition of isocyanides to p-quinone methides in the presence of BF
Identifiants
pubmed: 35986585
doi: 10.1002/asia.202200642
doi:
Substances chimiques
quinone methide
138230-21-4
Cyanides
0
Acetamides
0
Carbon Monoxide
7U1EE4V452
Indolequinones
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202200642Subventions
Organisme : CSIR-New Delhi
ID : HCP23
Organisme : CSIR, New Delhi
Organisme : UGC-New Delhi
Organisme : CSIR-NCL
Informations de copyright
© 2022 Wiley-VCH GmbH.
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