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A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines
We report the sustainable and efficient synthesis of a new type of quinoline derivatives bearing one or two SO(2)CF(3) groups. The protocol is metal‐, catalyst‐ and irradiation‐free, involves the use of readily available and stable precursors, and avoids the formation of side products. Also, the mil...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519061/ https://www.ncbi.nlm.nih.gov/pubmed/34369000 http://dx.doi.org/10.1002/chem.202102254 |
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author | Lázaro‐Milla, Carlos Almendros, Pedro |
author_facet | Lázaro‐Milla, Carlos Almendros, Pedro |
author_sort | Lázaro‐Milla, Carlos |
collection | PubMed |
description | We report the sustainable and efficient synthesis of a new type of quinoline derivatives bearing one or two SO(2)CF(3) groups. The protocol is metal‐, catalyst‐ and irradiation‐free, involves the use of readily available and stable precursors, and avoids the formation of side products. Also, the mild conditions of the process allow the tolerance of a wide range of functional groups. |
format | Online Article Text |
id | pubmed-8519061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85190612021-10-21 A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines Lázaro‐Milla, Carlos Almendros, Pedro Chemistry Communications We report the sustainable and efficient synthesis of a new type of quinoline derivatives bearing one or two SO(2)CF(3) groups. The protocol is metal‐, catalyst‐ and irradiation‐free, involves the use of readily available and stable precursors, and avoids the formation of side products. Also, the mild conditions of the process allow the tolerance of a wide range of functional groups. John Wiley and Sons Inc. 2021-08-10 2021-09-24 /pmc/articles/PMC8519061/ /pubmed/34369000 http://dx.doi.org/10.1002/chem.202102254 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Lázaro‐Milla, Carlos Almendros, Pedro A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines |
title | A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines |
title_full | A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines |
title_fullStr | A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines |
title_full_unstemmed | A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines |
title_short | A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines |
title_sort | convenient formal [4+2] heterocylization route to bis(triflyl)tetrahydroquinolines |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519061/ https://www.ncbi.nlm.nih.gov/pubmed/34369000 http://dx.doi.org/10.1002/chem.202102254 |
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