1167441-87-3Relevant academic research and scientific papers
Lewis acid-catalyzed double addition of indoles to ketones: Synthesis of bis(indolyl)methanes with all-carbon quaternary centers
Choi, Jeongin,Kook, Seunghoon,Lee, Sarah Yunmi,Lee, Si On
, p. 9060 - 9064 (2020)
We report herein a Lewis acid-catalyzed nucleophilic double-addition of indoles to ketones under mild conditions. This process occurs with various ketones ranging from dialkyl ketones to diaryl ketones, thereby providing access to an array of bis(indolyl)
An efficient Au(i) catalyst for double hydroarylation of alkynes with heteroarenes
Luo, Cuicui,Yang, Hongwei,Mao, Rongfang,Lu, Chunxu,Cheng, Guangbin
, p. 3417 - 3423 (2015/05/20)
An efficient Ph3PAuCl/AgOTf-catalyzed double hydroarylation of alkynes with heteroarenes was developed. Functional alkynes undergo double addition with simple heteroarenes such as pyrroles, furans and thiophenes under mild reaction conditions.
Synthesis of methanes having four different carbon substituents utilizing indium-catalyzed cleavage of carbon-pyrrolyl bonds
Tsuchimoto, Teruhisa,Ainoya, Taku,Aoki, Kazuki,Wagatsuma, Tatsuya,Shirakawa, Eiji
supporting information; experimental part, p. 2437 - 2440 (2009/09/06)
A pyrrolyl group bound to an sp3 carbon atom in gem-dipyrrolylalkanes was found to be successfully replaced by a certain range of carbon nucleophiles in the presence of an indium catalyst. The reaction can also be performed efficiently as a thr
