109932-97-0Relevant articles and documents
Photoinduced Cross-Coupling of Amines with 1,2-Diiodobenzene and Its Application in the Synthesis of Carbazoles
Zhao, Xinxin,Chen, Ming,Huang, Binbin,Yang, Chao,Gao, Yuan,Xia, Wujiong
supporting information, p. 2981 - 2989 (2018/05/15)
A facile and efficient process for the preparation of various tertiary aminobenzenes and carbazole derivatives via photoinduced cross-coupling of amines with 1,2-diiodobenzene is reported. Mechanistic investigations indicate that the transformation proceeds via nucleo-philic addition of an amine to the benzyne intermediate accompanied with a proton transfer process, followed by an oxidative cyclization of the generated diphenylamine to furnish the corresponding carbazole products.
Photoreactions with a Twist: Atropisomerism-Driven Divergent Reactivity of Enones with UV and Visible Light
Vallavoju, Nandini,Sreenithya, Avadakkam,Ayitou, Anoklase J.-L.,Jockusch, Steffen,Sunoj, Raghavan B.,Sivaguru, Jayaraman
supporting information, p. 11339 - 11348 (2016/08/03)
Light-induced transformation of atropisomeric and achiral enones displays divergent reactivity. Photocyclization leading to 3,4-dihydroquinolin-2-one was observed with achiral enone carboxamide, whereas the atropisomeric enone carboxamides underwent hydro
Palladium-catalyzed amidation of unactivated c(sp3)-h bonds: From anilines to indolines
Neumann, Julia J.,Rakshit, Souvik,Droge, Thomas,Glorius, Frank
supporting information; experimental part, p. 6892 - 6895 (2009/12/26)
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