Skip to main content
. 2014 Dec 12;56(5):666–673. doi: 10.1016/j.tetlet.2014.12.012

Table 2.

Comparison of preparative methods of 3,3-di(indolyl)indolin-2-ones with various reported catalysts

graphic file with name fx3.jpg

Entry Catalyst Reaction conditions Time (h/min) Yield (%) Refs.
1 Ionic liquid 60 mol % of ([BMIM][BF4]LiCl), rt 1 h 93 16a
2 Bismuth(III) Triflate 2 mol %, CH3CN, rt 3 h 92 16b
3 Indium(III) acetylacetonate 10 mol %,(H2O:CH3CN 4:1), rt 2.5 h 92 16c
4 Silica sulfuric acid 0.2 g, CH2Cl2, rt 2 h 92 16d
5 Ruthenium trichloride 5 mol %, MeOH, 50 °C 2 h 75 16f
6 Ceric ammonium nitrate (CAN) 10 mol %, US, EtOH, rt 3 h 95 16g
7 I2 (Iodine) 10 mol %, CH2Cl2, rt 14 h 82 16h
8 KSF 0.1 g, reflux in EtOH 0.5 h 90 16i
9 β-CD-SO3H 10 mol %, H2O, reflux 5 min 96 This work