83515-10-0Relevant articles and documents
Multi-site cyclization via initial C-H activation using a rhodium(III) catalyst: Rapid assembly of frameworks containing indoles and indolines
Huang, Ji-Rong,Qin, Liu,Zhu, Yu-Qin,Song, Qiang,Dong, Lin
, p. 2844 - 2847 (2015)
Tandem multi-site cyclization triggered by Rh(III)-catalyzed C-H activation has been achieved for highly efficient synthesis of spirocycle indolin-3-one (C2-cyclization), benzo[a]carbazole (C3-cyclization) and an unusual indoxyl core (N1-cyclization). In particular, the synthesis of pseudo-indoxyl is typically completed within 10 min, and the reaction tolerates air, water and a range of solvents.
An asymmetric normal-electron-demand aza-Diels-Alder reaction via trienamine catalysis
Liu, Jing-Xin,Zhou, Qing-Qing,Deng, Jin-Gen,Chen, Ying-Chun
, p. 8175 - 8178 (2013/12/04)
An asymmetric normal-electron-demand aza-Diels-Alder cycloaddition of 2-aryl-3H-indol-3-ones and 2,4-dienals was explored via trienamine catalysis of a chiral secondary amine. Multifunctional tricyclic polyhydropyrido[1,2-a] indoles were efficiently constructed in good stereoselectivity (up to 92% ee, >19:1 dr).
Synthesis and Reactions of 2-Phenylindol-3-ones
Hiremath, Shivayogi P.,Biradar, Jaiprakash S.,Mruthyunjayaswamy, B. H. M.
, p. 308 - 310 (2007/10/02)
2-Phenyl-3-aminoindoles (2a-d) have been synthesised and converted into the corresponding 2-phenylindol-3-ones (4a-d), which on reaction with o-phenylenediamine (5a,b) and nitrostyrene give 9-substituted 5H-5a,6-dihydro-5a-phenylindoloquinoxalines