Palladium-catalyzed amidation of carbazole derivatives via hydroamination of isocyanates.
Org Biomol Chem
; 22(30): 6090-6094, 2024 Jul 31.
Article
em En
| MEDLINE
| ID: mdl-39005158
ABSTRACT
The first amidation of carbazoles at the N9 position via palladium-catalyzed hydroamination of isocyanates is demonstrated. This simple, general and efficient method could deliver a wide range of carbazole-N-carboxamides in up to 99% yield. The salient features of this transformation include simple conditions with no need for a strong base, high chemo- and regio-selectivities and good functional group tolerance. In particular, this work-up-free and chromatography-free protocol is time-saving, cost-effective and user-friendly.
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Base de dados:
MEDLINE
Idioma:
En
Ano de publicação:
2024
Tipo de documento:
Article
País de afiliação:
China