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3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches

Aziridination reactions represent a powerful tool in aziridine synthesis. Significant progress has been achieved in this field in the last decades, whereas highly functionalized aziridines including 3-arylated aziridine-2-carbonyl compounds play an important role in both medical and synthetic chemis...

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Autores principales: Strumfs, Boriss, Uljanovs, Romans, Velikijs, Kirils, Trapencieris, Peteris, Strumfa, Ilze
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469611/
https://www.ncbi.nlm.nih.gov/pubmed/34576025
http://dx.doi.org/10.3390/ijms22189861
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author Strumfs, Boriss
Uljanovs, Romans
Velikijs, Kirils
Trapencieris, Peteris
Strumfa, Ilze
author_facet Strumfs, Boriss
Uljanovs, Romans
Velikijs, Kirils
Trapencieris, Peteris
Strumfa, Ilze
author_sort Strumfs, Boriss
collection PubMed
description Aziridination reactions represent a powerful tool in aziridine synthesis. Significant progress has been achieved in this field in the last decades, whereas highly functionalized aziridines including 3-arylated aziridine-2-carbonyl compounds play an important role in both medical and synthetic chemistry. For the reasons listed, in the current review we have focused on the ways to obtain 3-arylated aziridines and on the recent advances (mainly since the year 2000) in the methodology of the synthesis of these compounds via aziridination.
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spelling pubmed-84696112021-09-27 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches Strumfs, Boriss Uljanovs, Romans Velikijs, Kirils Trapencieris, Peteris Strumfa, Ilze Int J Mol Sci Review Aziridination reactions represent a powerful tool in aziridine synthesis. Significant progress has been achieved in this field in the last decades, whereas highly functionalized aziridines including 3-arylated aziridine-2-carbonyl compounds play an important role in both medical and synthetic chemistry. For the reasons listed, in the current review we have focused on the ways to obtain 3-arylated aziridines and on the recent advances (mainly since the year 2000) in the methodology of the synthesis of these compounds via aziridination. MDPI 2021-09-13 /pmc/articles/PMC8469611/ /pubmed/34576025 http://dx.doi.org/10.3390/ijms22189861 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Strumfs, Boriss
Uljanovs, Romans
Velikijs, Kirils
Trapencieris, Peteris
Strumfa, Ilze
3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches
title 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches
title_full 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches
title_fullStr 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches
title_full_unstemmed 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches
title_short 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches
title_sort 3-arylaziridine-2-carboxylic acid derivatives and (3-arylaziridin-2-yl)ketones: the aziridination approaches
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469611/
https://www.ncbi.nlm.nih.gov/pubmed/34576025
http://dx.doi.org/10.3390/ijms22189861
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