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One-Pot Synthesis of Aminated Benzo-Fused Heterocycles and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann Type Reaction
[Image: see text] We report here a direct and effective method to synthesize a primary amine of several polycyclic aromatic compounds. This reaction has been achieved through copper (I)-catalyzed Ullmann C–N coupling. Furthermore, this strategy allows the synthesis of new N-substituted dibenzothioph...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931392/ https://www.ncbi.nlm.nih.gov/pubmed/33681638 http://dx.doi.org/10.1021/acsomega.1c00414 |
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author | Alelaiwi, Sawsan H. McKee, James R. |
author_facet | Alelaiwi, Sawsan H. McKee, James R. |
author_sort | Alelaiwi, Sawsan H. |
collection | PubMed |
description | [Image: see text] We report here a direct and effective method to synthesize a primary amine of several polycyclic aromatic compounds. This reaction has been achieved through copper (I)-catalyzed Ullmann C–N coupling. Furthermore, this strategy allows the synthesis of new N-substituted dibenzothiophene derivatives through the coupling of 2-bromodibenzothiophene with various ranges of primary and secondary amines. The use of inexpensive catalysts, aqueous ammonia as the convenient source of ammonia and ligand free, makes this protocol environmentally and economically favorable for the synthesis of these compounds. |
format | Online Article Text |
id | pubmed-7931392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79313922021-03-05 One-Pot Synthesis of Aminated Benzo-Fused Heterocycles and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann Type Reaction Alelaiwi, Sawsan H. McKee, James R. ACS Omega [Image: see text] We report here a direct and effective method to synthesize a primary amine of several polycyclic aromatic compounds. This reaction has been achieved through copper (I)-catalyzed Ullmann C–N coupling. Furthermore, this strategy allows the synthesis of new N-substituted dibenzothiophene derivatives through the coupling of 2-bromodibenzothiophene with various ranges of primary and secondary amines. The use of inexpensive catalysts, aqueous ammonia as the convenient source of ammonia and ligand free, makes this protocol environmentally and economically favorable for the synthesis of these compounds. American Chemical Society 2021-02-15 /pmc/articles/PMC7931392/ /pubmed/33681638 http://dx.doi.org/10.1021/acsomega.1c00414 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under an ACS AuthorChoice License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Alelaiwi, Sawsan H. McKee, James R. One-Pot Synthesis of Aminated Benzo-Fused Heterocycles and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann Type Reaction |
title | One-Pot Synthesis of Aminated Benzo-Fused Heterocycles
and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann
Type Reaction |
title_full | One-Pot Synthesis of Aminated Benzo-Fused Heterocycles
and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann
Type Reaction |
title_fullStr | One-Pot Synthesis of Aminated Benzo-Fused Heterocycles
and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann
Type Reaction |
title_full_unstemmed | One-Pot Synthesis of Aminated Benzo-Fused Heterocycles
and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann
Type Reaction |
title_short | One-Pot Synthesis of Aminated Benzo-Fused Heterocycles
and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann
Type Reaction |
title_sort | one-pot synthesis of aminated benzo-fused heterocycles
and n-substituted dibenzothiophenes via copper-catalyzed ullmann
type reaction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931392/ https://www.ncbi.nlm.nih.gov/pubmed/33681638 http://dx.doi.org/10.1021/acsomega.1c00414 |
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