1160044-47-2Relevant academic research and scientific papers
The mechanism of N-vinylindole formation via tandem imine formation and cycloisomerisation of o-ethynylanilines
Kennedy, Danielle F.,Nova, Ainara,Willis, Anthony C.,Eisenstein, Odile,Messerle, Barbara A.
, p. 10296 - 10304 (2009)
The reaction of 2-(2-phenylethynyl)aniline with acetone in presence of [IrCp*Cl2]2 has previously been found to yield a vinyl indole derivative and not the indole expected to form following a hydroamination reaction. Experimental dat
Application of UV-Vis spectroscopy to high throughput screening of hydroamination catalysts
Kennedy, Danielle F.,Messerle, Barbara A.,Rumble, Sarah L.
experimental part, p. 818 - 824 (2009/06/19)
Potential catalysts for the hydroamination of 2-(2-phenylethynyl)aniline 2 which have been identified through high throughput screening methods were investigated. Two complexes were shown to be highly active hydroamination catalysts in acetone: the in situ combinations of [Rh(CO)2Cl] 2-mesBIAN-NaBF4 (mesBIAN = bis(2,4,6-trimethylphenylimino) acenapthene) and [Ir(COD)Cl]2-NaBF4 (COD = 1,5-cyclooctadiene). The isolated complexes [M(N-N)XCl]BF4 (M = Rh, Ir; N-N = bidentate nitrogen donor ligand; X = CO or Cp*) were found to be inactive as catalysts for the conversion of 2 to 3. However, chloride abstraction from these complexes through the addition of AgBF4 was found to generate extremely active catalysts. Particularly active was the complex [Rh(CO)ClmesBIAN]-AgBF4 (5 mol%) which achieved complete conversion of 2 to 3 in 12 minutes at 50 °C. Also identified was the formation of the unusual product, N-(2-methylvinyl)-2-phenylindole 5, catalysed by [IrCp*Cl2]2-NaBF4 from starting material 2via the incorporation of one molecule of acetone.
