1160847-23-3Relevant articles and documents
Scalable Electrochemical Transition-Metal-Free Dehydrogenative Cross-Coupling Amination Enabled Alkaloid Clausines Synthesis
Zhang, Pan,Li, Baoying,Niu, Liwei,Wang, Ling,Zhang, Guofeng,Jia, Xiaofei,Zhang, Guoying,Liu, Siyuan,Ma, Li,Gao, Wei,Qin, Dawei,Chen, Jianbin
supporting information, p. 2342 - 2347 (2020/05/05)
Reported herein is an environmentally benign electrochemical C?H bond dehydrogenative amination protocol for the construction of privileged carbazole moiety with broad generality. Preliminary mechanistic investigations implied a radical reaction pathway.
A direct palladium-catalyzed route to selectively substituted carbazoles through sequential C-C and C-N bond formation: Synthesis of carbazomycin A
Della Ca', Nicola,Sassi, Giovanni,Catellani, Marta
supporting information; experimental part, p. 2179 - 2182 (2009/10/02)
The present paper offers a synthetically simple one-pot procedure for the catalytic preparation of the biologically interesting class of carbazoles. The new procedure is based on the combined catalysis of palladium and norbornene starting from o-substituted iodoarenes and N-sulfonylated or N-acetylated o-bromoanilines. A well-known member of this class, carbazomycin A, has been successfully prepared.
