173442-64-3Relevant academic research and scientific papers
Synthesis of 1,2-fused indoles by radical cyclisation
Moody, Christopher J.,Norton, Claire L.
, p. 2639 - 2643 (2007/10/03)
Treatment of the 1-(ω-iodoalkyl)indole-3-carbaldehydes 8-13 with tributyltin hydride and AIBN results in radical cyclisation to give the 1,2-fused indoles 14-19 containing five-, six- and seven-membered rings. The tetrahydropyridoindole 18 is converted into the indolequinone 23.
Synthesis of 1,2-fused indoles by radical cyclisation
Moody, Christopher J.,Norton, Claire L.
, p. 9051 - 9052 (2007/10/02)
Treatment of the 1-(ω-iodoalkyl)indole-3-carboxaldehydes 8-13 with tributyltin hydride and AIBN results in radical cyclisation with oxidation to given the 1,2-fused indoles 14-19.
