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Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents
An effective and clean FC alkylation of indoles and electron-rich arenes with β-nitroalkenes in HFIP was reported. The desired products are formed rapidly in excellent yields under mild conditions without the need for any additional catalysts or reagents. Further, this methodology can be applied to...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078892/ https://www.ncbi.nlm.nih.gov/pubmed/35540471 http://dx.doi.org/10.1039/c8ra01397g |
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author | Tang, Ren-Jin Milcent, Thierry Crousse, Benoit |
author_facet | Tang, Ren-Jin Milcent, Thierry Crousse, Benoit |
author_sort | Tang, Ren-Jin |
collection | PubMed |
description | An effective and clean FC alkylation of indoles and electron-rich arenes with β-nitroalkenes in HFIP was reported. The desired products are formed rapidly in excellent yields under mild conditions without the need for any additional catalysts or reagents. Further, this methodology can be applied to one-pot synthesis of biologically active tryptamine derivatives. |
format | Online Article Text |
id | pubmed-9078892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90788922022-05-09 Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents Tang, Ren-Jin Milcent, Thierry Crousse, Benoit RSC Adv Chemistry An effective and clean FC alkylation of indoles and electron-rich arenes with β-nitroalkenes in HFIP was reported. The desired products are formed rapidly in excellent yields under mild conditions without the need for any additional catalysts or reagents. Further, this methodology can be applied to one-pot synthesis of biologically active tryptamine derivatives. The Royal Society of Chemistry 2018-03-13 /pmc/articles/PMC9078892/ /pubmed/35540471 http://dx.doi.org/10.1039/c8ra01397g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Tang, Ren-Jin Milcent, Thierry Crousse, Benoit Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents |
title | Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents |
title_full | Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents |
title_fullStr | Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents |
title_full_unstemmed | Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents |
title_short | Friedel–Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents |
title_sort | friedel–crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078892/ https://www.ncbi.nlm.nih.gov/pubmed/35540471 http://dx.doi.org/10.1039/c8ra01397g |
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