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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MDPI AG
2021-09-01
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author | Boriss Strumfs Romans Uljanovs Kirils Velikijs Peteris Trapencieris Ilze Strumfa |
author_facet | Boriss Strumfs Romans Uljanovs Kirils Velikijs Peteris Trapencieris Ilze Strumfa |
author_sort | Boriss Strumfs |
collection | DOAJ |
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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format | Article |
id | doaj.art-fdd484e8eb2747fa83cbad71f96d3435 |
institution | Directory Open Access Journal |
issn | 1661-6596 1422-0067 |
language | English |
last_indexed | 2024-03-10T07:36:21Z |
publishDate | 2021-09-01 |
publisher | MDPI AG |
record_format | Article |
series | International Journal of Molecular Sciences |
spelling | doaj.art-fdd484e8eb2747fa83cbad71f96d34352023-11-22T13:28:42ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-09-012218986110.3390/ijms221898613-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination ApproachesBoriss Strumfs0Romans Uljanovs1Kirils Velikijs2Peteris Trapencieris3Ilze Strumfa4Latvian Institute of Organic Synthesis, 21 Aizkraukles Street, LV-1006 Riga, LatviaDepartment of Pathology, Riga Stradins University, 16 Dzirciema Street, LV-1007 Riga, LatviaDepartment of Pathology, Riga Stradins University, 16 Dzirciema Street, LV-1007 Riga, LatviaLatvian Institute of Organic Synthesis, 21 Aizkraukles Street, LV-1006 Riga, LatviaDepartment of Pathology, Riga Stradins University, 16 Dzirciema Street, LV-1007 Riga, LatviaAziridination 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.https://www.mdpi.com/1422-0067/22/18/9861aziridinesaziridinationiminescarbenesnitrenes |
spellingShingle | Boriss Strumfs Romans Uljanovs Kirils Velikijs Peteris Trapencieris Ilze Strumfa 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches International Journal of Molecular Sciences aziridines aziridination imines carbenes nitrenes |
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 | aziridines aziridination imines carbenes nitrenes |
url | https://www.mdpi.com/1422-0067/22/18/9861 |
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