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http://hdl.handle.net/2445/128411| Title: | Fischer indole reaction in batch and flow employing a sulfonic acid resin: synthesis of pyrido[2,3-a]carbazoles |
| Author: | Bosch, Caroline López-Lledó, Pablo Bonjoch i Sesé, Josep Bradshaw, Ben Nieuwland, Pieter J. Blanco-Ania, Daniel Rutjes, Floris P. J. T. |
| Keywords: | Síntesi en fase sólida Compostos heterocíclics Àcids orgànics Síntesi orgànica Solid-phase synthesis Heterocyclic compounds Organic acids Organic synthesis |
| Issue Date: | 31-May-2016 |
| Abstract: | An Amberlite IR 120 H-promoted one-pot Fischer indolization from a cis-decahydroquinoline using a range of phenylhydrazines led to compounds with the pyrido[2,3-a]carbazole scaffold. The process may be conducted either in batch mode or in a continuous manner in a flow reactor. The stereochemical course of the Fischer indole reaction changed in going from using free phenylhydrazine to the corresponding hydrochloride in batch conditions, whereas, with the short reaction times in continuous flow, no changes due to isomerization processes were observed. Keywords: Fischer indole synthesis, one-pot synthesis, continuous-flow synthesis, sulfonic acid resin, immobilized reagents, pyrido[2,3-a]carbazoles |
| Note: | https://doi.org/10.1556/1846.2016.00016 |
| It is part of: | Journal Of Flow Chemistry, 2016, vol. 6, num. 3, p. 240-243 |
| URI: | http://hdl.handle.net/2445/128411 |
| Related resource: | https://doi.org/10.1556/1846.2016.00016 |
| ISSN: | 2062-249X |
| Appears in Collections: | Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica) Articles publicats en revistes (Institut de Biomedicina (IBUB)) |
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| 666640.pdf | 3.64 MB | Adobe PDF | View/Open |
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