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A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines
A simple synthetic strategy has been developed for the synthesis of 2- and 1-alkyl/aryl/dialkylaminoquinolines and isoquinolines from the easily available quinoline and isoquinoline-N-oxides, different amines, triflic anhydride as activating agent and acetonitrile as solvent in a one-pot reaction un...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049819/ https://www.ncbi.nlm.nih.gov/pubmed/35492149 http://dx.doi.org/10.1039/c9ra10397j |
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author | Nanaji, Yerramsetti Kirar, Seema Pawar, Sandip V. Yadav, Ashok Kumar |
author_facet | Nanaji, Yerramsetti Kirar, Seema Pawar, Sandip V. Yadav, Ashok Kumar |
author_sort | Nanaji, Yerramsetti |
collection | PubMed |
description | A simple synthetic strategy has been developed for the synthesis of 2- and 1-alkyl/aryl/dialkylaminoquinolines and isoquinolines from the easily available quinoline and isoquinoline-N-oxides, different amines, triflic anhydride as activating agent and acetonitrile as solvent in a one-pot reaction under metal-free conditions at 0 °C to room temperature. |
format | Online Article Text |
id | pubmed-9049819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90498192022-04-29 A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines Nanaji, Yerramsetti Kirar, Seema Pawar, Sandip V. Yadav, Ashok Kumar RSC Adv Chemistry A simple synthetic strategy has been developed for the synthesis of 2- and 1-alkyl/aryl/dialkylaminoquinolines and isoquinolines from the easily available quinoline and isoquinoline-N-oxides, different amines, triflic anhydride as activating agent and acetonitrile as solvent in a one-pot reaction under metal-free conditions at 0 °C to room temperature. The Royal Society of Chemistry 2020-02-20 /pmc/articles/PMC9049819/ /pubmed/35492149 http://dx.doi.org/10.1039/c9ra10397j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Nanaji, Yerramsetti Kirar, Seema Pawar, Sandip V. Yadav, Ashok Kumar A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines |
title | A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines |
title_full | A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines |
title_fullStr | A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines |
title_full_unstemmed | A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines |
title_short | A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines |
title_sort | mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049819/ https://www.ncbi.nlm.nih.gov/pubmed/35492149 http://dx.doi.org/10.1039/c9ra10397j |
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